Allele Registry

Canonical Allele Identifier: PA2830001048

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV004012454

ClinVar Variation:

3073912

HGVS (amino-acid)	Matching Registered Transcripts
NP_077744.4:p.Arg61Gly	CA064702 NM_024426.6:c.181C>G