Canonical Allele Identifier: PA645460081
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 372089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Lys26Met
CA8677141
NM_058216.3:c.77A>T