Allele Registry

Canonical Allele Identifier: PA2825161330

Gene: WT1 HGNC NCBI

ClinVar Variation Id: 2926856

HGVS (amino-acid)	Matching Registered Transcripts
NP_000369.4:p.Met302Ile	CA379962181 NM_000378.6:c.906G>T CA379962182 NM_000378.6:c.906G>C CA379962183 NM_000378.6:c.906G>A