Canonical Allele Identifier: PA916001413
Gene: NONO HGNC NCBI

Linked Data

ClinVar Variation Id: 427778
ClinVar RCV Id: RCV000490794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031389.3:p.Gly391Cys
CA413548646
NM_007363.5:c.1171G>T