Canonical Allele Identifier: PA2829391922
Gene: RAD51C HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Ala22Glu
CA400336836
NM_002876.4:c.65C>A
CA3057228019
NM_002876.4:c.63_65delinsTGA