Allele Registry

Canonical Allele Identifier: PA2830002016

Gene: WT1 HGNC NCBI

ClinVar Allele:

178637

ClinVar RCV:

RCV000157583

RCV000892804

RCV002492615

RCV003162657

RCV004551354

ClinVar Variation:

180586

HGVS (amino-acid)	Matching Registered Transcripts
NP_077744.4:p.Met255Lys	CA016452 NM_024426.6:c.764T>A