Allele Registry

Canonical Allele Identifier: PA2830000040

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003673

ClinVar Variation:

3499

HGVS (amino-acid)	Matching Registered Transcripts
NP_077742.3:p.Ser346Gly	CA016356 NM_024424.5:c.1036A>G