Allele Registry

Canonical Allele Identifier: PA2825161669

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV003412544

ClinVar Variation:

2637933

HGVS (amino-acid)	Matching Registered Transcripts
NP_000369.4:p.Asp452Ala	CA379958829 NM_000378.6:c.1355A>C