Canonical Allele Identifier: PA348865
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 220140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Lys320Asn
CA348863
NM_058216.3:c.960G>C
CA400361589
NM_058216.3:c.960G>T