Allele Registry

Canonical Allele Identifier: PA2830000487

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003677

ClinVar Variation:

3502

HGVS (amino-acid)	Matching Registered Transcripts
NP_077742.3:p.Phe456Leu	CA016305 NM_024424.5:c.1366T>C CA379958982 NM_024424.5:c.1368C>G CA379958984 NM_024424.5:c.1368C>A