Allele Registry

Canonical Allele Identifier: PA2826130559

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000144154

RCV000522954

RCV000636307

RCV000678845

RCV001266283

RCV003992195

ClinVar Variation:

156106

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171455.1:p.Arg1576Gln	CA170757 NM_001177984.2:c.4727G>A