Canonical Allele Identifier: PA2829999034
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1502337
ClinVar RCV Id: RCV002010960 RCV004011114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Val88Ile
CA379966049
NM_024424.5:c.262G>A