Allele Registry

Canonical Allele Identifier: PA2830002644

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003680

RCV001288153

ClinVar Variation:

3505

HGVS (amino-acid)	Matching Registered Transcripts
NP_077744.4:p.Arg439Cys	CA016279 NM_024426.6:c.1315C>T