Allele Registry

Canonical Allele Identifier: PA2825161661

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV003883245

ClinVar Variation:

3024186

HGVS (amino-acid)	Matching Registered Transcripts
NP_000369.4:p.Arg450Leu	CA379958847 NM_000378.6:c.1349G>T