Allele Registry

Canonical Allele Identifier: PA2830000472

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003672

RCV001280531

RCV001879755

ClinVar Variation:

3498

973193

HGVS (amino-acid)	Matching Registered Transcripts
NP_077742.3:p.His446Gln	CA016292 NM_024424.5:c.1338C>G CA379959168 NM_024424.5:c.1338C>A