Canonical Allele Identifier: CA120542
Gene:

Linked Data

ClinVar Variation Id: 9557
dbSNP Id: rs199474674
MyVariant Identifiers: chrMT:g.5532G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5532G>A , J01415.2:m.5532G>A GRCh38