Allele Registry

Canonical Allele Identifier: PA2825161655

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003679

ClinVar Variation:

3504

HGVS (amino-acid)	Matching Registered Transcripts
NP_000369.4:p.Phe448Leu	CA016316 NM_000378.6:c.1342T>C CA379958865 NM_000378.6:c.1344C>G CA379958866 NM_000378.6:c.1344C>A