Allele Registry

Canonical Allele Identifier: PA2826129535

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV001091243

ClinVar Variation:

871344

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171455.1:p.Ile268Phe	CA385226553 NM_001177984.2:c.802A>T