Allele Registry

Canonical Allele Identifier: PA2825160556

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV004012454

ClinVar Variation:

3073912

HGVS (amino-acid)	Matching Registered Transcripts
NP_000369.4:p.Arg61Gly	CA064702 NM_000378.6:c.181C>G