Allele Registry

Canonical Allele Identifier: PA2830000462

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003680

RCV001288153

ClinVar Variation:

3505

HGVS (amino-acid)	Matching Registered Transcripts
NP_077742.3:p.Arg439Cys	CA016279 NM_024424.5:c.1315C>T