Canonical Allele Identifier: PA116266
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_001185480.1:p.Asp252Asn
CA016338
NM_001198551.1:c.754G>A
CA2695202602
NM_001198551.1:c.753_754delinsGA