Canonical Allele Identifier: PA2829392068
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 1018619
ClinVar RCV Id: RCV001317946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Ser47Asn
CA400337821
NM_002876.4:c.140G>A