Canonical Allele Identifier: PA2830282742
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 3195749
ClinVar RCV Id: RCV004489558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Glu421Gln
CA340878061
NM_144573.4:c.1261G>C