Canonical Allele Identifier: PA116254
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3487
ClinVar RCV Id: RCV000003656 RCV000003658 RCV000003657 RCV000467701 RCV000484426 RCV001003819 RCV001290016 RCV002293973 RCV002482821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Arg250Trp
CA016324
NM_001198551.1:c.748C>T