Canonical Allele Identifier: CA337096449
Gene:

Linked Data

dbSNP Id: rs199993153
MyVariant Identifiers: chrMT:g.3200T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3200T>C , J01415.2:m.3200T>C GRCh38