Canonical Allele Identifier: PA2828361586
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2430619
ClinVar RCV Id: RCV003129152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Ser1838Phe
CA384888247
NM_001369788.1:c.5513C>T