Allele Registry

Canonical Allele Identifier: PA2826129479

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000239765

RCV001268591

ClinVar Variation:

253276

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171455.1:p.Gly214Asp	CA10586285 NM_001177984.2:c.641G>A