Canonical Allele Identifier: CA337097195
Gene:

Linked Data

ClinVar Variation Id: 689949
ClinVar RCV Id: RCV000850805
dbSNP Id: rs28619345
MyVariant Identifiers: chrMT:g.5590G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5590G>A , J01415.2:m.5590G>A GRCh38