Allele Registry

Canonical Allele Identifier: PA116262

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003660

RCV001376854

ClinVar Variation:

3489

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185480.1:p.Asp252Gly	CA016344 NM_001198551.1:c.755A>G