Canonical Allele Identifier: PA2829998747
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1484861
ClinVar RCV Id: RCV002030257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Leu23Phe
CA379966454
NM_024424.5:c.67C>T