Allele Registry

Canonical Allele Identifier: PA2828361211

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000144155

RCV003753672

ClinVar Variation:

156107

2907429

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356717.1:p.Asn1425Lys	CA170758 NM_001369788.1:c.4275C>A CA384908571 NM_001369788.1:c.4275C>G