Canonical Allele Identifier: PA2826062609
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 1502758
ClinVar RCV Id: RCV002045249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165780.1:p.Gly377Cys
CA340878643
NM_001172309.2:c.1129G>T