Allele Registry

Canonical Allele Identifier: PA116290

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003672

RCV001280531

RCV001879755

ClinVar Variation:

3498

973193

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185480.1:p.His229Gln	CA016292 NM_001198551.1:c.687C>G CA379959168 NM_001198551.1:c.687C>A