Canonical Allele Identifier: PA2829391914
Gene: RAD51C HGNC NCBI

Linked Data

ClinVar Variation Id: 142510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Pro21Leu
CA168555
NM_002876.4:c.62C>T