{{Rsnum
|rsid=80315385
|Chromosome=12
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CACNA1C
|position=2504932
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CACNA1C
}}{{omim
|id=114205
|rsnum=80315385
|variant=0002
}}{{ClinVar
|rsid=80315385
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=2614098
|CHROM=12
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=CACNA1C:775
|GENE_NAME=CACNA1C
|GENE_ID=775
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.2614098G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1403; 114205.0002
|CLNSIG=5
|CLNCUI=C1832916; C1832916
|CLNDBN=Timothy syndrome; not provided
|Disease=Timothy syndrome; not provided
|CLNACC=RCV000019200.22; RCV000058284.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1403:C1832916:601005:65283:768
}}{{PMID|15863612|OA=1
}} Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations.

{{PMID|15863612|OA=1
}} Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations.