Canonical Allele Identifier: PA645491589
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 373625
ClinVar RCV Id: RCV000414636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Tyr22Cys
CA16042401
NM_144573.4:c.65A>G