Allele Registry

Canonical Allele Identifier: PA2826129815

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000500414

RCV001857161

RCV002259344

ClinVar Variation:

436671

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171455.1:p.Ser627Leu	CA385229785 NM_001177984.2:c.1880C>T