Allele Registry

Canonical Allele Identifier: PA2828276034

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV003883245

ClinVar Variation:

3024186

HGVS (amino-acid)	Matching Registered Transcripts
NP_001354783.1:p.Arg71Leu	CA379958847 NM_001367854.1:c.212G>T