Allele Registry

Canonical Allele Identifier: PA2826224313

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000208133

RCV003223623

ClinVar Variation:

222890

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185481.1:p.Gly188Val	CA351790 NM_001198552.2:c.563G>T