Allele Registry

Canonical Allele Identifier: PA2830000483

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003667

RCV000003668

RCV002512715

ClinVar Variation:

3495

HGVS (amino-acid)	Matching Registered Transcripts
NP_077742.3:p.His450Tyr	CA016298 NM_024424.5:c.1348C>T