Allele Registry

Canonical Allele Identifier: PA2826224373

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003677

ClinVar Variation:

3502

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185481.1:p.Phe222Leu	CA016305 NM_001198552.2:c.664T>C CA379958982 NM_001198552.2:c.666C>G CA379958984 NM_001198552.2:c.666C>A