Allele Registry

Canonical Allele Identifier: PA2827292138

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000285972

ClinVar Variation:

195689

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317189.1:p.Asn1329Asp	CA242214 NM_001330260.2:c.3985A>G