Canonical Allele Identifier: PA2826222663
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 847109
ClinVar RCV Id: RCV001050583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185480.1:p.Thr102Asn
CA219496195
NM_001198551.1:c.305C>A