Canonical Allele Identifier: PA2826062524
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 1302226
ClinVar RCV Id: RCV001754115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165780.1:p.Leu317Phe
CA340876864
NM_001172309.2:c.951A>C
CA340876867
NM_001172309.2:c.951A>T