Allele Registry

Canonical Allele Identifier: PA916075519

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000122313

RCV000231832

RCV001107195

RCV001107196

RCV001107197

RCV003460864

ClinVar Variation:

135455

HGVS (amino-acid)	Matching Registered Transcripts
NP_077744.4:p.Arg385Gln	CA016505 NM_024426.6:c.1154G>A