Allele Registry

Canonical Allele Identifier: PA916047014

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003679

ClinVar Variation:

3504

HGVS (amino-acid)	Matching Registered Transcripts
NP_001354783.1:p.Phe69Leu	CA016316 NM_001367854.1:c.205T>C CA379958865 NM_001367854.1:c.207C>G CA379958866 NM_001367854.1:c.207C>A