Canonical Allele Identifier: PA2829998742
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073049
ClinVar RCV Id: RCV004015063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Thr22Lys
CA379966458
NM_024424.5:c.65C>A