Allele Registry

Canonical Allele Identifier: PA2830000403

Gene: WT1 HGNC NCBI

ClinVar Variation Id: 406697

HGVS (amino-acid)	Matching Registered Transcripts
NP_077742.3:p.Asn404Thr	CA064353 NM_024424.5:c.1211A>C