Allele Registry

Canonical Allele Identifier: PA2826222765

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV001941410

ClinVar Variation:

1442038

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185480.1:p.Ser129Cys	CA379960501 NM_001198551.1:c.385A>T CA2573146222 NM_001198551.1:c.384_385delinsAT