Canonical Allele Identifier: CA120544
Gene:

Linked Data

ClinVar Variation Id: 9560
dbSNP Id: rs118203888
MyVariant Identifiers: chrMT:g.12258C>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12258C>A , J01415.2:m.12258C>A GRCh38