Canonical Allele Identifier: PA2580368885
Gene: NONO HGNC NCBI

Linked Data

ClinVar Variation Id: 1723686
ClinVar RCV Id: RCV002308960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031389.3:p.Gly436Val
CA413550087
NM_007363.5:c.1307G>T