Canonical Allele Identifier: CA337098675
Gene:

Linked Data

dbSNP Id: rs878889554
MyVariant Identifiers: chrMT:g.10035T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10035T>C , J01415.2:m.10035T>C GRCh38