Canonical Allele Identifier: PA2826062950
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 229056
ClinVar RCV Id: RCV000222628 RCV000768811 RCV001359679 RCV002415903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165780.1:p.Gly597Arg
CA10576435
NM_001172309.2:c.1789G>A
CA340883349
NM_001172309.2:c.1789G>C