Canonical Allele Identifier: PA2826130755
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1315611
ClinVar RCV Id: RCV001755273

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Val1814Asp
CA384887577
NM_001177984.2:c.5441T>A