Allele Registry

Canonical Allele Identifier: PA116258

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003659

RCV000484493

RCV001250546

RCV001851622

RCV002243617

RCV002496247

RCV003147274

ClinVar Variation:

3488

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185480.1:p.Arg222His	CA016285 NM_001198551.1:c.665G>A