Canonical Allele Identifier: PA2826130666
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 374665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.His1686Gln
CA16043838
NM_001177984.2:c.5058C>A
CA384884291
NM_001177984.2:c.5058C>G