Canonical Allele Identifier: PA2828361560
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1036977
ClinVar RCV Id: RCV001340057
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Ile1823Val
CA384887832
NM_001369788.1:c.5467A>G