Canonical Allele Identifier: PA2827292824
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1040115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Lys1880Glu
CA384888255
NM_001330260.2:c.5638A>G