{{Rsnum
|rsid=121908218
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CACNA1A
|position=13303576
|Gene_s=CACNA1A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=121908218
|Reversed=1
|FwdREF=C
|FwdALT=A,G
|REF=G
|ALT=C,T
|RSPOS=13414390
|CHROM=19
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=CACNA1A:773
|GENE_NAME=CACNA1A
|GENE_ID=773
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000019.9:g.13414390G>C; NC_000019.9:g.13414390G>T
|CLNSRC=UniProtKB (variants); OMIM Allelic Variant
|CLNSRCID=VAR_043827; 601011.0010
|CLNSIG=5
|CLNCUI=C1832894; C1832894
|CLNDBN=Familial hemiplegic migraine type 1
|Disease=Familial hemiplegic migraine type 1
|CLNACC=RCV000059293.1; RCV000009020.2
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1388:C1832894:141500:569
|CLNORIGIN=1
}}{{PMID Auto
|PMID=11439943
|Title=The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
}}