Canonical Allele Identifier: PA2825891361
Gene: NONO HGNC NCBI

Linked Data

ClinVar Variation Id: 2832251
ClinVar RCV Id: RCV003689411

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138881.1:p.Arg469Cys
CA413550707
NM_001145409.2:c.1405C>T