Canonical Allele Identifier: PA658808684
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 520368
ClinVar RCV Id: RCV000618386 RCV001066584
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Asp478Asn
CA340879355
NM_144573.4:c.1432G>A