Allele Registry

Canonical Allele Identifier: PA2826129524

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000478102

ClinVar Variation:

420906

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171455.1:p.Leu257Val	CA16619558 NM_001177984.2:c.769C>G