Allele Registry

Canonical Allele Identifier: PA2830000452

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003669

RCV002512716

ClinVar Variation:

3496

HGVS (amino-acid)	Matching Registered Transcripts
NP_077742.3:p.Cys433Gly	CA016265 NM_024424.5:c.1297T>G