Canonical Allele Identifier: PA2826130800
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1391051
ClinVar RCV Id: RCV001889702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Ser1841Pro
CA384888285
NM_001177984.2:c.5521T>C