Canonical Allele Identifier: PA2829392508
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 2109914
ClinVar RCV Id: RCV003020109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Pro127Leu
CA400341891
NM_002876.4:c.380C>T