Canonical Allele Identifier: PA891863788
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476694
ClinVar RCV Id: RCV000552982 RCV002258969 RCV003459255
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Ser67Cys
CA379966175
NM_024426.6:c.200C>G