Allele Registry

Canonical Allele Identifier: PA916047009

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003677

ClinVar Variation:

3502

HGVS (amino-acid)	Matching Registered Transcripts
NP_001354783.1:p.Phe60Leu	CA016305 NM_001367854.1:c.178T>C CA379958982 NM_001367854.1:c.180C>G CA379958984 NM_001367854.1:c.180C>A