Allele Registry

Canonical Allele Identifier: PA2826224132

Gene: WT1 HGNC NCBI

ClinVar Variation Id: 406687

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185481.1:p.Phe133Cys	CA064143 NM_001198552.2:c.398T>G