Canonical Allele Identifier: PA2499297544
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 1014582

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Arg57del
CA739076541
NM_144573.4:c.170_172del