Canonical Allele Identifier: PA891863772
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 406699
ClinVar RCV Id: RCV000457233
ClinVar Variation Id: 1512513
ClinVar RCV Id: RCV002023068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Thr12Pro
CA064742
NM_024426.6:c.34A>C
CA2573146221
NM_024426.6:c.33_34delinsAC