Canonical Allele Identifier: PA2828361638
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 461349
ClinVar RCV Id: RCV000553439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Arg1891Trp
CA6571955
NM_001369788.1:c.5671C>T