Canonical Allele Identifier: PA2826062618
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 1963363
ClinVar RCV Id: RCV002711112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165780.1:p.Leu394Phe
CA24686520
NM_001172309.2:c.1182G>T
CA340879092
NM_001172309.2:c.1182G>C