Canonical Allele Identifier: CA645373343

Gene:

Linked Data

• ClinVar Variation Id: 430687
• ClinVar RCV Id: RCV000494972
• dbSNP Id: rs1131692061
• MyVariant Identifiers: chrMT:g.12271T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12271T>C , J01415.2:m.12271T>C	GRCh38