Canonical Allele Identifier: PA891863869
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_077744.4:p.Tyr400His
CA064344
NM_024426.6:c.1198T>C