Allele Registry

Canonical Allele Identifier: PA116306

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003680

RCV001288153

ClinVar Variation:

3505

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185480.1:p.Arg222Cys	CA016279 NM_001198551.1:c.664C>T