Canonical Allele Identifier: PA2829999200
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2406757
ClinVar RCV Id: RCV002754724 RCV004009556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Ser123Ala
CA379965838
NM_024424.5:c.367T>G