Canonical Allele Identifier: PA2830000397
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3492
ClinVar RCV Id: RCV000003664
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Cys403Tyr
CA016258
NM_024424.5:c.1208G>A