Allele Registry

Canonical Allele Identifier: PA2825161385

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV001941410

ClinVar Variation:

1442038

HGVS (amino-acid)	Matching Registered Transcripts
NP_000369.4:p.Ser329Cys	CA379960501 NM_000378.6:c.985A>T CA2573146222 NM_000378.6:c.984_985delinsAT