Canonical Allele Identifier: PA2829999047
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1448032
ClinVar RCV Id: RCV002012045 RCV004010975
ClinVar Variation Id: 2056056
ClinVar RCV Id: RCV002910204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Gly96dup
CA2580084184
NM_024424.5:c.288_289insGGA