Canonical Allele Identifier: PA1139750449
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 933906
ClinVar RCV Id: RCV001202216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Thr176Ile
CA379964768
NM_024426.6:c.527C>T