Canonical Allele Identifier: PA2829999191
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 651615
ClinVar RCV Id: RCV000807017 RCV003325521 RCV004001692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ala120Thr
CA379965859
NM_024424.5:c.358G>A