Canonical Allele Identifier: PA2830000752
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073651
ClinVar RCV Id: RCV004016657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Phe3Val
CA2790963050
NM_024426.6:c.7T>G