Allele Registry

Canonical Allele Identifier: PA2830002765

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003679

ClinVar Variation:

3504

HGVS (amino-acid)	Matching Registered Transcripts
NP_077744.4:p.Phe465Leu	CA016316 NM_024426.6:c.1393T>C CA379958865 NM_024426.6:c.1395C>G CA379958866 NM_024426.6:c.1395C>A