Allele Registry

Canonical Allele Identifier: PA2829998902

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000346620

RCV000393616

RCV000465825

RCV000709153

RCV001931279

RCV003165825

ClinVar Variation:

304429

1426420

HGVS (amino-acid)	Matching Registered Transcripts
NP_077742.3:p.Ser54Arg	CA064646 NM_024424.5:c.162C>G CA379966253 NM_024424.5:c.162C>A CA379966259 NM_024424.5:c.160A>C