Canonical Allele Identifier: PA2499290209
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1057387
ClinVar RCV Id: RCV001366357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ser11Cys
CA379966529
NM_024426.6:c.32C>G