Allele Registry

Canonical Allele Identifier: PA2827292251

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000685228

ClinVar Variation:

565622

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317189.1:p.Asn1466Ser	CA384908570 NM_001330260.2:c.4397A>G