Canonical Allele Identifier: PA2829998921
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 855555
ClinVar RCV Id: RCV001060840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Arg57His
CA379966237
NM_024424.5:c.170G>A