Allele Registry

Canonical Allele Identifier: PA2826224270

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003664

ClinVar Variation:

3492

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185481.1:p.Cys169Tyr	CA016258 NM_001198552.2:c.506G>A