Canonical Allele Identifier: PA891863771
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 543119
ClinVar RCV Id: RCV000653782 RCV002257918 RCV002493051 RCV003228973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ala10Tyr
CA658797616
NM_024426.6:c.28_29delinsTA