Allele Registry

Canonical Allele Identifier: PA2830002775

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV003883245

ClinVar Variation:

3024186

HGVS (amino-acid)	Matching Registered Transcripts
NP_077744.4:p.Arg467Leu	CA379958847 NM_024426.6:c.1400G>T