Allele Registry

Canonical Allele Identifier: PA2826224415

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003661

RCV000003662

RCV003322746

ClinVar Variation:

3490

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185481.1:p.Asp235Asn	CA016338 NM_001198552.2:c.703G>A CA2695202602 NM_001198552.2:c.702_703delinsGA