Allele Registry

Canonical Allele Identifier: PA645449502

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000488921

ClinVar Variation:

427167

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Ile1631Asn	CA384880452 NM_014191.4:c.4892T>A