Allele Registry

Canonical Allele Identifier: PA2826223459

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV003412544

ClinVar Variation:

2637933

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185480.1:p.Asp252Ala	CA379958829 NM_001198551.1:c.755A>C