Canonical Allele Identifier: PA658670902
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 482167
ClinVar Variation Id: 1762833
ClinVar RCV Id: RCV002430344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_478123.1:p.Val28Leu
CA400337090
NM_058216.3:c.82G>C
CA400337095
NM_058216.3:c.82G>T