Canonical Allele Identifier: PA2742009807
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 2691225
ClinVar RCV Id: RCV003487251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Ser15Pro
CA340884938
NM_144573.4:c.43T>C