Allele Registry

Canonical Allele Identifier: PA916047019

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003660

RCV001376854

ClinVar Variation:

3489

HGVS (amino-acid)	Matching Registered Transcripts
NP_001354783.1:p.Asp73Gly	CA016344 NM_001367854.1:c.218A>G