{{Rsnum
|rsid=121908215
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CACNA1A
|position=13359707
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CACNA1A
}}{{omim
|id=601011
|rsnum=121908215
|variant=0009
}}{{ClinVar
|rsid=121908215
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=13470521
|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.13470521C>T
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=601011.0009; VAR_043825
|CLNSIG=5
|CLNCUI=C0752124; C1720416
|CLNDBN=Spinocerebellar ataxia 6; Episodic ataxia type 2
|Disease=Spinocerebellar ataxia 6; Episodic ataxia type 2
|CLNACC=RCV000009018.3; RCV000009019.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1140:C0752124:183086; NBK1501:C1720416:108500:97:420932006
}}{{PMID Auto
|PMID=9345107
|Title=Progressive ataxia due to a missense mutation in a calcium-channel gene.
|OA=1
}}

{{PMID Auto
|PMID=14718690
|Title=Clinical spectrum of episodic ataxia type 2.
}}