{{Rsnum
|rsid=80338789
|Chromosome=17
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN4A
|position=63947091
|Gene_s=SCN4A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80338789
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=62024451
|CHROM=17
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=SCN4A:6329
|GENE_NAME=SCN4A
|GENE_ID=6329
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.62024451C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1338; 603967.0030
|CLNSIG=5
|CLNCUI=CN031165
|CLNDBN=Hypokalemic periodic paralysis 1; Hypokalemic periodic paralysis, type 2
|Disease=Hypokalemic periodic paralysis 1; Hypokalemic periodic paralysis
|CLNACC=RCV000020270.1; RCV000043510.2
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1338:NBK1496:CN031165:170400:681; NBK1338:C2750061:613345:681
}}{{PMID Auto
|PMID=16890191
|Title=Gating defects of a novel Na+ channel mutant causing hypokalemic periodic paralysis.
}}