Canonical Allele Identifier: PA2829392019
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 185535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Leu39Val
CA192210
NM_002876.4:c.115C>G