Canonical Allele Identifier: PA183793
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 179137
ClinVar RCV Id: RCV000155922 RCV002390360
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Ile477Ser
CA183791
NM_144573.4:c.1430T>G