{{Rsnum
|rsid=80338777
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CACNA1S
|position=201077915
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CACNA1S
}}{{omim
|id=114208
|rsnum=80338777
|variant=0003
}}{{ClinVar
|rsid=80338777
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=201077915
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000a05000002110100
|GENEINFO=CACNA1S:779
|GENE_NAME=CACNA1S
|GENE_ID=779
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.201077915C>T
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000069.2:c.1583G>A; NBK1338; 114208.0003
|CLNSIG=5
|CLNCUI=CN031165; CN031165
|CLNDBN=Hypokalemic periodic paralysis 1
|Disease=Hypokalemic periodic paralysis 1
|CLNACC=RCV000019192.22
|Tags=RV;PM;PMC;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1338:NBK1496:CN031165:170400:ORPHA681
}}{{PMID Auto
|PMID=7847370
|Title=Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families.
|OA=1
}}

{{PMID Auto
|PMID=7897626
|Title=Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis.
|OA=1
}}

{{PMID Auto
|PMID=7987325
|Title=A calcium channel mutation causing hypokalemic periodic paralysis.
}}

{{PMID Auto
|PMID=10074484
|Title=Impairment of skeletal muscle adenosine triphosphate-sensitive K+ channels in patients with hypokalemic periodic paralysis.
|OA=1
}}

{{PMID Auto
|PMID=11353725
|Title=Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A.
}}