Allele Registry

Canonical Allele Identifier: PA2830002073

Gene: WT1 HGNC NCBI

ClinVar RCV:

RCV000653789

RCV004004099

ClinVar Variation:

543126

HGVS (amino-acid)	Matching Registered Transcripts
NP_077744.4:p.Pro269Arg	CA065646 NM_024426.6:c.806C>G