Canonical Allele Identifier: PA2826062996
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 518918
ClinVar RCV Id: RCV000621846 RCV001868102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165780.1:p.Ile607Thr
CA919020
NM_001172309.2:c.1820T>C