Allele Registry

Canonical Allele Identifier: PA2826224345

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003680

RCV001288153

ClinVar Variation:

3505

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185481.1:p.Arg205Cys	CA016279 NM_001198552.2:c.613C>T