Canonical Allele Identifier: PA891863809
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476701
ClinVar RCV Id: RCV000533914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Pro127Thr
CA379965815
NM_024426.6:c.379C>A