Canonical Allele Identifier: PA2828360465
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1176942
ClinVar RCV Id: RCV001532692
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Glu468Lys
CA385228723
NM_001369788.1:c.1402G>A