Canonical Allele Identifier: PA338968
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 216807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Lys235Asn
CA338966
NM_058216.3:c.705G>T
CA400350187
NM_058216.3:c.705G>C