Allele Registry

Canonical Allele Identifier: PA116298

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003677

ClinVar Variation:

3502

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185480.1:p.Phe239Leu	CA016305 NM_001198551.1:c.715T>C CA379958982 NM_001198551.1:c.717C>G CA379958984 NM_001198551.1:c.717C>A