Allele Registry

Canonical Allele Identifier: PA2825161615

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003672

RCV001280531

RCV001879755

ClinVar Variation:

3498

973193

HGVS (amino-acid)	Matching Registered Transcripts
NP_000369.4:p.His429Gln	CA016292 NM_000378.6:c.1287C>G CA379959168 NM_000378.6:c.1287C>A