Allele Registry

Canonical Allele Identifier: PA658810899

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000653789

RCV004004099

ClinVar Variation:

543126

HGVS (amino-acid)	Matching Registered Transcripts
NP_001185480.1:p.Pro52Arg	CA065646 NM_001198551.1:c.155C>G