Allele Registry

Canonical Allele Identifier: PA2826224406

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV003883245

ClinVar Variation:

3024186

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185481.1:p.Arg233Leu	CA379958847 NM_001198552.2:c.698G>T