Allele Registry

Canonical Allele Identifier: PA163969

Gene: RAD51C HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

150654

ClinVar RCV:

RCV000129215

RCV000167882

RCV000409379

RCV000588471

RCV001778747

RCV001798436

RCV002509232

ClinVar Variation:

140940

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_478123.1:p.Glu45Gly	CA163967 NM_058216.3:c.134A>G