Canonical Allele Identifier: PA2826062674
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 179137
ClinVar RCV Id: RCV000155922 RCV002390360
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165780.1:p.Ile413Ser
CA183791
NM_001172309.2:c.1238T>G