Canonical Allele Identifier: PA2829830664
Gene: UPF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3186770
ClinVar RCV Id: RCV004482151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056357.1:p.Thr260Ile
CA5407241
NM_015542.4:c.779C>T