Canonical Allele Identifier: PA2580419666
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2190510
ClinVar RCV Id: RCV002616426

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060551.2:p.Ala118Glu
CA397858942
NM_018081.2:c.353C>A