Canonical Allele Identifier: PA2826224261
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 304419
ClinVar RCV Id: RCV000270479 RCV000332520 RCV000363180 RCV000653775 RCV003165824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185481.1:p.Tyr166His
CA064344
NM_001198552.2:c.496T>C