Canonical Allele Identifier: PA2826130793
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2430619
ClinVar RCV Id: RCV003129152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Ser1838Phe
CA384888247
NM_001177984.2:c.5513C>T