Allele Registry

Canonical Allele Identifier: PA116302

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003679

ClinVar Variation:

3504

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185480.1:p.Phe248Leu	CA016316 NM_001198551.1:c.742T>C CA379958865 NM_001198551.1:c.744C>G CA379958866 NM_001198551.1:c.744C>A