Canonical Allele Identifier: PA2826062608
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 1769795
ClinVar RCV Id: RCV002385578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165780.1:p.Arg375Lys
CA918859
NM_001172309.2:c.1124G>A