Canonical Allele Identifier: PA2829998743
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1353800
ClinVar RCV Id: RCV001863605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Thr22Ala
CA379966460
NM_024424.5:c.64A>G