Allele Registry

Canonical Allele Identifier: PA162812

Gene: WT1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

139192

ClinVar RCV:

RCV000122310

RCV000782221

RCV001081231

RCV001107940

RCV001107941

RCV001107942

RCV002255305

RCV002284191

RCV003588578

RCV004551194

ClinVar Variation:

135453

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185480.1:p.Pro37Ser	CA016444 NM_001198551.1:c.109C>T