Allele Registry

Canonical Allele Identifier: PA2830000285

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000122313

RCV000231832

RCV001107195

RCV001107196

RCV001107197

RCV003460864

ClinVar Variation:

135455

HGVS (amino-acid)	Matching Registered Transcripts
NP_077742.3:p.Arg385Gln	CA016505 NM_024424.5:c.1154G>A