Canonical Allele Identifier: PA2825861722
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 392640

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137463.1:p.Pro359Ser
CA8355254
NM_001143991.2:c.1075C>T