Allele Registry

Canonical Allele Identifier: PA2826224398

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003679

ClinVar Variation:

3504

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185481.1:p.Phe231Leu	CA016316 NM_001198552.2:c.691T>C CA379958865 NM_001198552.2:c.693C>G CA379958866 NM_001198552.2:c.693C>A