Canonical Allele Identifier: PA2825891355
Gene: NONO HGNC NCBI

Linked Data

ClinVar Variation Id: 2579951
ClinVar RCV Id: RCV003328926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138881.1:p.Ile444Thr
CA413550254
NM_001145409.2:c.1331T>C