Allele Registry

Canonical Allele Identifier: PA2828275998

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000208133

RCV003223623

ClinVar Variation:

222890

HGVS (amino-acid)	Matching Registered Transcripts
NP_001354783.1:p.Gly26Val	CA351790 NM_001367854.1:c.77G>T