Allele Registry

Canonical Allele Identifier: PA891855336

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000685228

ClinVar Variation:

565622

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Asn1466Ser	CA384908570 NM_014191.4:c.4397A>G