Canonical Allele Identifier: PA891863865
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 406692
ClinVar RCV Id: RCV000462501 RCV001107841 RCV001107842 RCV001107843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Arg375His
CA064260
NM_024426.6:c.1124G>A