Canonical Allele Identifier: PA2826062675
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 520368
ClinVar RCV Id: RCV000618386 RCV001066584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165780.1:p.Asp414Asn
CA340879355
NM_001172309.2:c.1240G>A