Canonical Allele Identifier: PA2830002791
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3490
ClinVar RCV Id: RCV000003661 RCV000003662 RCV003322746
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077744.4:p.Asp469Asn
CA016338
NM_024426.6:c.1405G>A
CA2695202602
NM_024426.6:c.1404_1405delinsGA