Canonical Allele Identifier: PA2826063013
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 841719
ClinVar RCV Id: RCV001043993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165780.1:p.Glu608Lys
CA919021
NM_001172309.2:c.1822G>A