Canonical Allele Identifier: PA2826130223
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 530412

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Lys1123Gln
CA384894017
NM_001177984.2:c.3367A>C