Allele Registry

Canonical Allele Identifier: PA645449412

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000420671

ClinVar Variation:

391391

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Phe1480Ile	CA16606654 NM_014191.4:c.4438T>A