Allele Registry

Canonical Allele Identifier: PA2826130608

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000189285

ClinVar Variation:

207127

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171455.1:p.Ala1609Val	CA318292 NM_001177984.2:c.4826C>T