Canonical Allele Identifier: CA337097176
Gene:

Linked Data

ClinVar Variation Id: 689946
ClinVar RCV Id: RCV000850802
dbSNP Id: rs200719361
MyVariant Identifiers: chrMT:g.5568A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5568A>G , J01415.2:m.5568A>G GRCh38