Allele Registry

Canonical Allele Identifier: PA2825161410

Gene: WT1 HGNC NCBI

ClinVar Allele:

50286

ClinVar RCV:

RCV000034780

RCV000122312

RCV000709139

RCV001081983

RCV002255123

RCV004549406

ClinVar Variation:

41847

HGVS (amino-acid)	Matching Registered Transcripts
NP_000369.4:p.Cys338Arg	CA016364 NM_000378.6:c.1012T>C