Canonical Allele Identifier: PA2829391906
Gene: RAD51C HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002867.1:p.Ser20Tyr
CA400336749
NM_002876.4:c.59C>A