Canonical Allele Identifier: CA658653725
Gene:

Linked Data

ClinVar Variation Id: 441080
ClinVar RCV Id: RCV000509159
dbSNP Id: rs1556424072
MyVariant Identifiers: chrMT:g.12170G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12170G>A , J01415.2:m.12170G>A GRCh38