Canonical Allele Identifier: PA2827088775
Gene: RAD51AP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2248084
ClinVar RCV Id: RCV004106753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308162.1:p.Arg1110Thr
CA1538650
NM_001321233.1:c.3329G>C