Allele Registry

Canonical Allele Identifier: PA2828361079

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000725891

RCV001034264

RCV002453700

ClinVar Variation:

207114

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356717.1:p.Ala1214Thr	CA318266 NM_001369788.1:c.3640G>A