Canonical Allele Identifier: PA1139749665
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 864517
ClinVar RCV Id: RCV001071726 RCV002489716 RCV003736969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Pro9Leu
CA219511559
NM_024426.6:c.26C>T