Allele Registry

Canonical Allele Identifier: PA2826223222

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV004550589

ClinVar Variation:

2629839

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185480.1:p.Gly205Asp	CA379959445 NM_001198551.1:c.614G>A