Allele Registry

Canonical Allele Identifier: PA2825161668

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000659253

RCV004547831

ClinVar Variation:

547167

HGVS (amino-acid)	Matching Registered Transcripts
NP_000369.4:p.Asp452Tyr	CA379958830 NM_000378.6:c.1354G>T