Canonical Allele Identifier: PA2830002191
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2924237
ClinVar RCV Id: RCV003785987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Cys308Tyr
CA379962145
NM_024426.6:c.923G>A