Canonical Allele Identifier: PA2826062735
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 3195769
ClinVar RCV Id: RCV004489578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165780.1:p.Met476Ile
CA340881455
NM_001172309.2:c.1428G>A
CA340881456
NM_001172309.2:c.1428G>C
CA340881457
NM_001172309.2:c.1428G>T