Canonical Allele Identifier: CA337100649
Gene:

Linked Data

dbSNP Id: rs35315169
MyVariant Identifiers: chrMT:g.16111C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.16111C>T , J01415.2:m.16111C>T GRCh38