Allele Registry

Canonical Allele Identifier: PA2825161662

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003663

RCV004547456

ClinVar Variation:

3491

HGVS (amino-acid)	Matching Registered Transcripts
NP_000369.4:p.Arg450Pro	CA016330 NM_000378.6:c.1349G>C