Allele Registry

Canonical Allele Identifier: PA916075529

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003669

RCV002512716

ClinVar Variation:

3496

HGVS (amino-acid)	Matching Registered Transcripts
NP_077744.4:p.Cys433Gly	CA016265 NM_024426.6:c.1297T>G