Allele Registry

Canonical Allele Identifier: PA2741873434

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV003412544

ClinVar Variation:

2637933

HGVS (amino-acid)	Matching Registered Transcripts
NP_001354783.1:p.Asp73Ala	CA379958829 NM_001367854.1:c.218A>C