Canonical Allele Identifier: PA299884
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 182834
ClinVar RCV Id: RCV000160922 RCV000206110 RCV000218584 RCV001798558 RCV003467268
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Thr132Arg
CA299882
NM_058216.3:c.395C>G