Canonical Allele Identifier: PA645460102
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 246163
ClinVar Variation Id: 818633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Val41Leu
CA10584579
NM_058216.3:c.121G>C
CA400337598
NM_058216.3:c.121G>T