Allele Registry

Canonical Allele Identifier: PA645449439

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000441856

ClinVar Variation:

377169

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Gln1501Lys	CA16603287 NM_014191.4:c.4501C>A