Canonical Allele Identifier: CA337097206
Gene:

Linked Data

ClinVar Variation Id: 689962
ClinVar RCV Id: RCV000850819
dbSNP Id: rs879226228
MyVariant Identifiers: chrMT:g.5633C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5633C>T , J01415.2:m.5633C>T GRCh38