Allele Registry

Canonical Allele Identifier: PA2828361133

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000285972

ClinVar Variation:

195689

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356717.1:p.Asn1288Asp	CA242214 NM_001369788.1:c.3862A>G