Allele Registry

Canonical Allele Identifier: PA891863871

Gene: WT1 HGNC NCBI

ClinVar Variation Id: 406697

HGVS (amino-acid)	Matching Registered Transcripts
NP_077744.4:p.Asn404Thr	CA064353 NM_024426.6:c.1211A>C