Allele Registry

Canonical Allele Identifier: PA2825161541

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003664

ClinVar Variation:

3492

HGVS (amino-acid)	Matching Registered Transcripts
NP_000369.4:p.Cys386Tyr	CA016258 NM_000378.6:c.1157G>A