Canonical Allele Identifier: PA1139735934
Gene: NONO HGNC NCBI

Linked Data

ClinVar Variation Id: 450018
ClinVar RCV Id: RCV000522264

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031389.3:p.Ala439dup
CA331037122
NM_007363.5:c.1315_1317dup