Canonical Allele Identifier: PA2828360441
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2016893
ClinVar RCV Id: RCV002834927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Leu422Gln
CA385228190
NM_001369788.1:c.1265T>A