Canonical Allele Identifier: PA2828360907
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1320842

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Lys1014Glu
CA236318521
NM_001369788.1:c.3040A>G