Canonical Allele Identifier: CA337095935
Gene:

Linked Data

dbSNP Id: rs368221863
MyVariant Identifiers: chrMT:g.742T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.742T>C , J01415.2:m.742T>C GRCh38