Canonical Allele Identifier: PA891863861
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 406687
ClinVar RCV Id: RCV000459964 RCV003463879 RCV004000751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Phe367Cys
CA064143
NM_024426.6:c.1100T>G