Canonical Allele Identifier: PA2826062634
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 47890
ClinVar RCV Id: RCV000041160 RCV000240639 RCV000491718 RCV000701648 RCV000621584 RCV001256889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165780.1:p.Glu406del
CA142113
NM_001172309.2:c.1215_1217del