Canonical Allele Identifier: PA2825891270
Gene: NONO HGNC NCBI

Linked Data

ClinVar Variation Id: 1723686
ClinVar RCV Id: RCV002308960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138880.1:p.Gly436Val
CA413550087
NM_001145408.2:c.1307G>T