Canonical Allele Identifier: PA2573272286
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1407531
ClinVar RCV Id: RCV001918493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060551.2:p.Glu117del
CA624865065
NM_018081.2:c.350_352del