Canonical Allele Identifier: CA337097200
Gene:

Linked Data

ClinVar Variation Id: 689953
ClinVar RCV Id: RCV000850810
dbSNP Id: rs369496446
MyVariant Identifiers: chrMT:g.5603C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5603C>T , J01415.2:m.5603C>T GRCh38