Allele Registry

Canonical Allele Identifier: PA2826130465

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000441856

ClinVar Variation:

377169

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171455.1:p.Gln1460Lys	CA16603287 NM_001177984.2:c.4378C>A