Allele Registry

Canonical Allele Identifier: PA2829391915

Gene: RAD51C HGNC NCBI

ClinVar Allele:

213342

ClinVar RCV:

RCV000198013

RCV000580606

ClinVar Variation:

216806

HGVS (amino-acid)	Matching Registered Transcripts
NP_002867.1:p.Pro21Ser	CA337583 NM_002876.4:c.61C>T