Canonical Allele Identifier: PA2829392092
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 182830

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Ile52Leu
CA299870
NM_002876.4:c.154A>C
CA400339550
NM_002876.4:c.154A>T