Allele Registry

Canonical Allele Identifier: PA2825160592

Gene: WT1 HGNC NCBI

ClinVar Allele:

461287

ClinVar RCV:

RCV000544002

RCV001591301

RCV002256394

RCV002491099

RCV002527933

ClinVar Variation:

476696

HGVS (amino-acid)	Matching Registered Transcripts
NP_000369.4:p.Gln73Leu	CA219511297 NM_000378.6:c.218A>T