Canonical Allele Identifier: PA2580142155
Gene: RAD51AP2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092688.1:p.Asp344Asn
CA345916182
NM_001099218.3:c.1030G>A