Allele Registry

Canonical Allele Identifier: PA2828360389

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000189260

RCV001807118

ClinVar Variation:

207105

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356717.1:p.Met367Val	CA318248 NM_001369788.1:c.1099A>G