Allele Registry

Canonical Allele Identifier: PA351793

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000208133

RCV003223623

ClinVar Variation:

222890

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185480.1:p.Gly205Val	CA351790 NM_001198551.1:c.614G>T