Allele Registry

Canonical Allele Identifier: PA645449205

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000439821

RCV000766191

RCV003992294

ClinVar Variation:

383545

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Gly964Arg	CA16607342 NM_014191.4:c.2890G>C