Canonical Allele Identifier: PA116278
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3495
ClinVar RCV Id: RCV000003667 RCV000003668 RCV002512715
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.His233Tyr
CA016298
NM_001198551.1:c.697C>T