Canonical Allele Identifier: PA2827088681
Gene: RAD51AP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2605925
ClinVar RCV Id: RCV004344580

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308162.1:p.Asp244Tyr
CA1539110
NM_001321233.1:c.730G>T