Allele Registry

Canonical Allele Identifier: PA2826129987

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000489752

ClinVar Variation:

427069

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171455.1:p.Val842Glu	CA384884736 NM_001177984.2:c.2525T>A