Allele Registry

Canonical Allele Identifier: PA2826224416

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV003412544

ClinVar Variation:

2637933

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185481.1:p.Asp235Ala	CA379958829 NM_001198552.2:c.704A>C