Canonical Allele Identifier: PA2829998865
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476683
ClinVar RCV Id: RCV000534991 RCV003126819 RCV003999461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Trp45Arg
CA379966318
NM_024424.5:c.133T>C
CA379966319
NM_024424.5:c.133T>A