Allele Registry

Canonical Allele Identifier: PA2830000545

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV003412544

ClinVar Variation:

2637933

HGVS (amino-acid)	Matching Registered Transcripts
NP_077742.3:p.Asp469Ala	CA379958829 NM_024424.5:c.1406A>C