Allele Registry

Canonical Allele Identifier: PA2827292262

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000415327

ClinVar Variation:

374375

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317189.1:p.Asn1468Ser	CA16043682 NM_001330260.2:c.4403A>G