Allele Registry

Canonical Allele Identifier: PA2828275999

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV004550589

ClinVar Variation:

2629839

HGVS (amino-acid)	Matching Registered Transcripts
NP_001354783.1:p.Gly26Asp	CA379959445 NM_001367854.1:c.77G>A