Canonical Allele Identifier: PA2828361594
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 656459
ClinVar RCV Id: RCV000812885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Ser1841Tyr
CA384888287
NM_001369788.1:c.5522C>A