Canonical Allele Identifier: CA337100593
Gene:

Linked Data

ClinVar Variation Id: 690248
ClinVar RCV Id: RCV000851142
dbSNP Id: rs200572753
MyVariant Identifiers: chrMT:g.15938C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15938C>T , J01415.2:m.15938C>T GRCh38