Canonical Allele Identifier: PA2742009816
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 2564024
ClinVar RCV Id: RCV003306353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Gln72Lys
CA340886040
NM_144573.4:c.214C>A