Canonical Allele Identifier: CA337100778
Gene:

Linked Data

dbSNP Id: rs386829282
MyVariant Identifiers: chrMT:g.16222C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.16222C>T , J01415.2:m.16222C>T GRCh38