Canonical Allele Identifier: PA2828361612
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 645276

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Arg1863His
CA6571942
NM_001369788.1:c.5588G>A