Canonical Allele Identifier: PA2573303313
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 1502758
ClinVar RCV Id: RCV002045249
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Gly441Cys
CA340878643
NM_144573.4:c.1321G>T