Allele Registry

Canonical Allele Identifier: PA891863874

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000208133

RCV003223623

ClinVar Variation:

222890

HGVS (amino-acid)	Matching Registered Transcripts
NP_077744.4:p.Gly422Val	CA351790 NM_024426.6:c.1265G>T