Canonical Allele Identifier: PA891863779
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543129
ClinVar RCV Id: RCV000653792 RCV000709154 RCV000988523 RCV001108129 RCV001108130 RCV003442007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Gly42Ser
CA064232
NM_024426.6:c.124G>A