Allele Registry

Canonical Allele Identifier: PA891863801

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000545211

RCV000709150

RCV000763735

RCV001568364

RCV003139859

RCV003459256

ClinVar Variation:

476699

HGVS (amino-acid)	Matching Registered Transcripts
NP_077744.4:p.Ala105Gly	CA219511175 NM_024426.6:c.314C>G