Canonical Allele Identifier: PA2829998688
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2079842
ClinVar RCV Id: RCV002998832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077742.3:p.Thr12Ala
CA219511507
NM_024424.5:c.34A>G