Allele Registry

Canonical Allele Identifier: PA916075483

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003673

ClinVar Variation:

3499

HGVS (amino-acid)	Matching Registered Transcripts
NP_077744.4:p.Ser346Gly	CA016356 NM_024426.6:c.1036A>G