Canonical Allele Identifier: CA337097202
Gene:

Linked Data

ClinVar Variation Id: 689955
ClinVar RCV Id: RCV000850812
dbSNP Id: rs878963919
MyVariant Identifiers: chrMT:g.5605A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5605A>G , J01415.2:m.5605A>G GRCh38