Canonical Allele Identifier: PA1139750332
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 944633
ClinVar RCV Id: RCV001215074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ser143Pro
CA379965677
NM_024426.6:c.427T>C