Canonical Allele Identifier: CA337097637
Gene:

Linked Data

dbSNP Id: rs879080411
MyVariant Identifiers: chrMT:g.7492C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7492C>T , J01415.2:m.7492C>T GRCh38