Canonical Allele Identifier: CA913179809
Gene:

Linked Data

ClinVar Variation Id: 689935
ClinVar RCV Id: RCV000850788
dbSNP Id: rs1603220016

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5543T>C , J01415.2:m.5543T>C GRCh38