Canonical Allele Identifier: PA2829392014
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 2698556
ClinVar RCV Id: RCV003507639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Leu39Arg
CA400337538
NM_002876.4:c.116T>G