Canonical Allele Identifier: PA2742009813
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 2537892
ClinVar RCV Id: RCV004311234
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Phe35Ser
CA340885404
NM_144573.4:c.104T>C