Canonical Allele Identifier: CA16603222

Gene:

Linked Data

• ClinVar Variation Id: 376964
• ClinVar RCV Id: RCV000426541 ; RCV000851027
• dbSNP Id: rs1057520099
• MyVariant Identifiers: chrMT:g.12175T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12175T>C , J01415.2:m.12175T>C	GRCh38