Canonical Allele Identifier: PA2826063021
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 1019679
ClinVar RCV Id: RCV001319151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165780.1:p.Ser609Gly
CA340883766
NM_001172309.2:c.1825A>G