Canonical Allele Identifier: PA2580516536
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 1742526
ClinVar RCV Id: RCV002335294

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Lys16Glu
CA340884954
NM_144573.4:c.46A>G