Canonical Allele Identifier: PA916047007
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3495
ClinVar RCV Id: RCV000003667 RCV000003668 RCV002512715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354783.1:p.His54Tyr
CA016298
NM_001367854.1:c.160C>T