Allele Registry

Canonical Allele Identifier: PA2826130443

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000420671

ClinVar Variation:

391391

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171455.1:p.Phe1439Ile	CA16606654 NM_001177984.2:c.4315T>A