Canonical Allele Identifier: PA2830282772
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 3195769
ClinVar RCV Id: RCV004489578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Met540Ile
CA340881455
NM_144573.4:c.1620G>A
CA340881456
NM_144573.4:c.1620G>C
CA340881457
NM_144573.4:c.1620G>T