Allele Registry

Canonical Allele Identifier: PA2829998943

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV004012454

ClinVar Variation:

3073912

HGVS (amino-acid)	Matching Registered Transcripts
NP_077742.3:p.Arg61Gly	CA064702 NM_024424.5:c.181C>G