Canonical Allele Identifier: CA254832
Gene:

Linked Data

ClinVar Variation Id: 9559
dbSNP Id: rs118203890
MyVariant Identifiers: chrMT:g.15950G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15950G>A , J01415.2:m.15950G>A GRCh38