Canonical Allele Identifier: PA2825861867
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1312936

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137464.1:p.Leu53Phe
CA287494898
NM_001143992.2:c.159G>T
CA397856800
NM_001143992.2:c.159G>C