Canonical Allele Identifier: PA2830000714
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 476692
ClinVar RCV Id: RCV000527759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Asn511Ile
CA379957492
NM_024424.5:c.1532A>T