{{Rsnum
|rsid=121908217
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CACNA1A
|position=13308452
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CACNA1A
}}{{omim
|id=601011
|rsnum=121908217
|variant=0018
}}{{ClinVar
|rsid=121908217
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=13419266
|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
|CLNHGVS=NC_000019.9:g.13419266C>T
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=601011.0018; VAR_043826
|CLNSIG=5
|CLNCUI=C1832894; C0752124
|CLNDBN=Familial hemiplegic migraine type 1; Migraine, sporadic hemiplegic; Spinocerebellar ataxia 6
|Disease=Familial hemiplegic migraine type 1; Migraine; Spinocerebellar ataxia 6
|CLNACC=RCV000009028.3; RCV000009029.2; RCV000009030.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen; GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1388:C1832894:141500:569; C1832903; NBK1140:C0752124:183086
}}{{PMID Auto
|PMID=11439943
|Title=The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.
}}