Canonical Allele Identifier: CA337100604
Gene:

Linked Data

ClinVar Variation Id: 690253
ClinVar RCV Id: RCV000851147
dbSNP Id: rs28535186
MyVariant Identifiers: chrMT:g.15942T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15942T>C , J01415.2:m.15942T>C GRCh38