Allele Registry

Canonical Allele Identifier: PA891863818

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000471816

RCV001770319

RCV002256256

ClinVar Variation:

406693

HGVS (amino-acid)	Matching Registered Transcripts
NP_077744.4:p.Pro141Ser	CA064922 NM_024426.6:c.421C>T