Allele Registry

Canonical Allele Identifier: PA645449045

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000478102

ClinVar Variation:

420906

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Leu257Val	CA16619558 NM_014191.4:c.769C>G