Allele Registry

Canonical Allele Identifier: PA168557

Gene: RAD51C HGNC NCBI

ClinVar Allele:

152224

ClinVar RCV:

RCV000131660

RCV000701475

RCV001762314

ClinVar Variation:

142510

HGVS (amino-acid)	Matching Registered Transcripts
NP_478123.1:p.Pro21Leu	CA168555 NM_058216.3:c.62C>T CA3060598014 NM_058216.3:c.62_63delinsTG