Canonical Allele Identifier: PA2826130766
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1036977
ClinVar RCV Id: RCV001340057

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Ile1823Val
CA384887832
NM_001177984.2:c.5467A>G