Canonical Allele Identifier: PA2828361664
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2631031
ClinVar RCV Id: RCV004531541
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Arg1925Lys
CA384890373
NM_001369788.1:c.5774G>A