Canonical Allele Identifier: CA340925
Gene:

Linked Data

ClinVar Variation Id: 9585
ClinVar RCV Id: RCV000010202
dbSNP Id: rs118192104
MyVariant Identifiers: chrMT:g.8361G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8361G>A , J01415.2:m.8361G>A GRCh38