Canonical Allele Identifier: PA2580516704
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 1771371
ClinVar RCV Id: RCV002396505
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Glu462Val
CA918867
NM_144573.4:c.1385A>T