Canonical Allele Identifier: PA335450
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 201936
ClinVar RCV Id: RCV000183675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653174.3:p.Cys667Tyr
CA335448
NM_144573.4:c.2000G>A