Canonical Allele Identifier: PA2825891345
Gene: NONO HGNC NCBI

Linked Data

ClinVar Variation Id: 427778
ClinVar RCV Id: RCV000490794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138881.1:p.Gly391Cys
CA413548646
NM_001145409.2:c.1171G>T