{{Rsnum
|rsid=121908236
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CACNA1A
|position=13359724
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CACNA1A
}}{{omim
|id=601011
|rsnum=121908236
|variant=0025
}}{{ClinVar
|rsid=121908236
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=13470538
|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.13470538C>T
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=601011.0025; VAR_043824
|CLNSIG=5
|CLNCUI=C1720416
|CLNDBN=Episodic ataxia type 2
|Disease=Episodic ataxia type 2
|CLNACC=RCV000009037.2
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1501:C1720416:108500:97:420932006
}}{{PMID|14718690}} Clinical spectrum of episodic ataxia type 2.