Canonical Allele Identifier: PA913198708
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 620630
ClinVar RCV Id: RCV000761158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Gly317Glu
CA379962044
NM_024426.6:c.950G>A