Canonical Allele Identifier: PA891863804
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 406698
ClinVar RCV Id: RCV000473635 RCV002305489 RCV004000754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Pro115Ser
CA16613338
NM_024426.6:c.343C>T