Canonical Allele Identifier: PA2826129899
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 139069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Ile700Leu
CA302743
NM_001177984.2:c.2098A>T
CA384878895
NM_001177984.2:c.2098A>C