Allele Registry

Canonical Allele Identifier: PA318328

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000189304

RCV001323177

ClinVar Variation:

207145

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Ile207Val	CA318327 NM_014191.4:c.619A>G