Canonical Allele Identifier: PA2828361589
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1040115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Lys1839Glu
CA384888255
NM_001369788.1:c.5515A>G