Canonical Allele Identifier: CA274532
Gene:

Linked Data

ClinVar Variation Id: 162370
ClinVar RCV Id: RCV000169781
dbSNP Id: rs786200951
MyVariant Identifiers: chrMT:g.5610G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5610G>A , J01415.2:m.5610G>A GRCh38