Canonical Allele Identifier: PA2825861898
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1407531
ClinVar RCV Id: RCV001918493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137464.1:p.Glu117del
CA624865065
NM_001143992.2:c.350_352del