Canonical Allele Identifier: PA2741986902
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2679626
ClinVar RCV Id: RCV003464884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ile361Val
CA379960337
NM_024426.6:c.1081A>G