Allele Registry

Canonical Allele Identifier: PA2825161630

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003677

ClinVar Variation:

3502

HGVS (amino-acid)	Matching Registered Transcripts
NP_000369.4:p.Phe439Leu	CA016305 NM_000378.6:c.1315T>C CA379958982 NM_000378.6:c.1317C>G CA379958984 NM_000378.6:c.1317C>A