Canonical Allele Identifier: CA913179855
Gene:

Linked Data

ClinVar Variation Id: 689940
ClinVar RCV Id: RCV000850794
dbSNP Id: rs1603220022

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5557T>C , J01415.2:m.5557T>C GRCh38