Allele Registry

Canonical Allele Identifier: PA288620

Gene: RAD51C HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

133659

ClinVar RCV:

RCV000116171

RCV000212951

RCV000227763

RCV000302331

RCV000662871

RCV000709519

RCV001704017

ClinVar Variation:

128202

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_478123.1:p.Arg368Trp	CA288618 NM_058216.3:c.1102C>T