Canonical Allele Identifier: PA2826062624
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_001165780.1:p.Glu398Val
CA918867
NM_001172309.2:c.1193A>T