Allele Registry

Canonical Allele Identifier: PA2826130437

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000480970

RCV000988848

RCV001856819

ClinVar Variation:

418482

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171455.1:p.Gly1435Ser	CA16619563 NM_001177984.2:c.4303G>A