Allele Registry

Canonical Allele Identifier: PA916047018

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000659253

RCV004547831

ClinVar Variation:

547167

HGVS (amino-acid)	Matching Registered Transcripts
NP_001354783.1:p.Asp73Tyr	CA379958830 NM_001367854.1:c.217G>T