Canonical Allele Identifier: PA335458
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 201940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Arg475del
CA335456
NM_144573.4:c.1419_1421del
CA2646274716
NM_144573.4:c.1422_1424del