Allele Registry

Canonical Allele Identifier: PA2830000038

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV001941410

ClinVar Variation:

1442038

HGVS (amino-acid)	Matching Registered Transcripts
NP_077742.3:p.Ser346Cys	CA379960501 NM_024424.5:c.1036A>T CA2573146222 NM_024424.5:c.1035_1036delinsAT