Allele Registry

Canonical Allele Identifier: PA2830000170

Gene: WT1 HGNC NCBI

ClinVar Variation Id: 406687

HGVS (amino-acid)	Matching Registered Transcripts
NP_077742.3:p.Phe367Cys	CA064143 NM_024424.5:c.1100T>G