Allele Registry

Canonical Allele Identifier: PA916047005

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003680

RCV001288153

ClinVar Variation:

3505

HGVS (amino-acid)	Matching Registered Transcripts
NP_001354783.1:p.Arg43Cys	CA016279 NM_001367854.1:c.127C>T