Canonical Allele Identifier: PA658671048
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 480492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Thr121del
CA658658639
NM_058216.3:c.361_363del