Canonical Allele Identifier: CA259740

Gene:

Linked Data

• ClinVar Variation Id: 30004
• ClinVar RCV Id: RCV000022899 ; RCV000851039 ; RCV003319172
• dbSNP Id: rs387906733
• MyVariant Identifiers: chrMT:g.12201T>C (hg38)
• PubMed: PMID:21931169

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12201T>C , J01415.2:m.12201T>C	GRCh38