Canonical Allele Identifier: PA2826062653
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 201940
ClinVar RCV Id: RCV000183679 RCV000249380 RCV000458753 RCV001704886 RCV000845464 RCV001170730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165780.1:p.Arg411del
CA335456
NM_001172309.2:c.1227_1229del
CA2646274716
NM_001172309.2:c.1230_1232del