Canonical Allele Identifier: PA2827292935
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_001317189.1:p.Arg1966Lys
CA384890373
NM_001330260.2:c.5897G>A