Allele Registry

Canonical Allele Identifier: PA2825862055

Gene: WRAP53 HGNC NCBI

ClinVar RCV:

RCV000023967

ClinVar Variation:

30976

HGVS (amino-acid)	Matching Registered Transcripts
NP_001137464.1:p.His376Tyr	CA342771 NM_001143992.2:c.1126C>T