Canonical Allele Identifier: PA2826129949
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1445748
ClinVar RCV Id: RCV001992661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Val784Ile
CA384880194
NM_001177984.2:c.2350G>A