Allele Registry

Canonical Allele Identifier: PA2826224414

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003660

RCV001376854

ClinVar Variation:

3489

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185481.1:p.Asp235Gly	CA016344 NM_001198552.2:c.704A>G