Allele Registry

Canonical Allele Identifier: PA645449394

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000438505

RCV002298587

ClinVar Variation:

383869

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Lys1471Gln	CA16606653 NM_014191.4:c.4411A>C