Allele Registry

Canonical Allele Identifier: PA2830002174

Gene: WT1 HGNC NCBI

ClinVar Variation Id: 2926856

HGVS (amino-acid)	Matching Registered Transcripts
NP_077744.4:p.Met302Ile	CA379962181 NM_024426.6:c.906G>T CA379962182 NM_024426.6:c.906G>C CA379962183 NM_024426.6:c.906G>A