Canonical Allele Identifier: CA337097235
Gene:

Linked Data

ClinVar Variation Id: 689986
ClinVar RCV Id: RCV000850844
dbSNP Id: rs878999194
MyVariant Identifiers: chrMT:g.5780G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5780G>A , J01415.2:m.5780G>A GRCh38