Canonical Allele Identifier: CA254846

Gene:

Linked Data

• ClinVar Variation Id: 9630
• ClinVar RCV Id: RCV000010258 ; RCV000224305
• dbSNP Id: rs267606620
• MyVariant Identifiers: chrMT:g.1291T>C (hg38)
• PubMed: PMID:16458854

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.1291T>C , J01415.2:m.1291T>C	GRCh38