Allele Registry

Canonical Allele Identifier: PA116278

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003667

RCV000003668

RCV002512715

ClinVar Variation:

3495

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185480.1:p.His233Tyr	CA016298 NM_001198551.1:c.697C>T