Canonical Allele Identifier: PA2825891353
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_001138881.1:p.Gly436Val
CA413550087
NM_001145409.2:c.1307G>T