Canonical Allele Identifier: CA337097225
Gene:

Linked Data

ClinVar Variation Id: 689979
ClinVar RCV Id: RCV000850836
dbSNP Id: rs2854138
MyVariant Identifiers: chrMT:g.5711A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5711A>G , J01415.2:m.5711A>G GRCh38