Canonical Allele Identifier: PA2826062614
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 47888
ClinVar RCV Id: RCV001215702 RCV000041158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165780.1:p.Gly392Arg
CA142107
NM_001172309.2:c.1174G>A
CA340879026
NM_001172309.2:c.1174G>C