Canonical Allele Identifier: PA2741986859
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2940962
ClinVar RCV Id: RCV003792224
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Cys180Tyr
CA379964735
NM_024426.6:c.539G>A