Allele Registry

Canonical Allele Identifier: PA346787

Gene: WT1 HGNC NCBI

ClinVar Allele:

178637

ClinVar RCV:

RCV000157583

RCV000892804

RCV002492615

RCV003162657

RCV004551354

ClinVar Variation:

180586

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185480.1:p.Met38Lys	CA016452 NM_001198551.1:c.113T>A