Allele Registry

Canonical Allele Identifier: PA2825161659

Gene: WT1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000003656

RCV000003657

RCV000003658

RCV000467701

RCV000484426

RCV001003819

RCV001290016

RCV002293973

RCV002482821

ClinVar Variation:

3487

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000369.4:p.Arg450Trp	CA016324 NM_000378.6:c.1348C>T