Canonical Allele Identifier: CA274531
Gene:

Linked Data

ClinVar Variation Id: 162369
dbSNP Id: rs786200950
MyVariant Identifiers: chrMT:g.5631G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5631G>A , J01415.2:m.5631G>A GRCh38