Canonical Allele Identifier: PA2830002703
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.His450Tyr
CA016298
NM_024426.6:c.1348C>T