Canonical Allele Identifier: CA120548
Gene:

Linked Data

ClinVar Variation Id: 9569
dbSNP Id: rs387906419
MyVariant Identifiers: chrMT:g.7497G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7497G>A , J01415.2:m.7497G>A GRCh38