Canonical Allele Identifier: PA2829392497
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 409836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Gly125Ser
CA8677201
NM_002876.4:c.373G>A