Canonical Allele Identifier: PA2828361573
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1213776

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Glu1830Asp
CA384888049
NM_001369788.1:c.5490G>C
CA384888052
NM_001369788.1:c.5490G>T