Allele Registry

Canonical Allele Identifier: PA2825161384

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000003673

ClinVar Variation:

3499

HGVS (amino-acid)	Matching Registered Transcripts
NP_000369.4:p.Ser329Gly	CA016356 NM_000378.6:c.985A>G