Canonical Allele Identifier: PA891863770
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476686
ClinVar RCV Id: RCV000548802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ala10Ile
CA658658041
NM_024426.6:c.28_29delinsAT