Allele Registry

Canonical Allele Identifier: PA2828361213

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000144156

ClinVar Variation:

156108

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356717.1:p.Asn1425Thr	CA170759 NM_001369788.1:c.4274A>C