Allele Registry

Canonical Allele Identifier: PA2829392018

Gene: RAD51C HGNC NCBI

ClinVar RCV:

RCV003176623

ClinVar Variation:

2447777

HGVS (amino-acid)	Matching Registered Transcripts
NP_002867.1:p.Leu39Pro	CA400337535 NM_002876.4:c.116T>C CA3057228771 NM_002876.4:c.114_116delinsGCC CA3057228842 NM_002876.4:c.114_116delinsACC