Canonical Allele Identifier: PA2829998636
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2930682
ClinVar RCV Id: RCV003789992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Leu6Pro
CA379966565
NM_024424.5:c.17T>C