Allele Registry

Canonical Allele Identifier: PA2830002793

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV003412544

ClinVar Variation:

2637933

HGVS (amino-acid)	Matching Registered Transcripts
NP_077744.4:p.Asp469Ala	CA379958829 NM_024426.6:c.1406A>C