Canonical Allele Identifier: PA645460281
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 231486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Asp242Asn
CA10580749
NM_058216.3:c.724G>A