Canonical Allele Identifier: CA120538
Gene:

Linked Data

ClinVar Variation Id: 9550
dbSNP Id: rs118203891
MyVariant Identifiers: chrMT:g.5874T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5874T>C , J01415.2:m.5874T>C GRCh38