Allele Registry

Canonical Allele Identifier: PA645449269

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000417447

RCV001030824

ClinVar Variation:

392657

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Lys1237Arg	CA6571667 NM_014191.4:c.3710A>G