Allele Registry

Canonical Allele Identifier: PA093529

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000144155

RCV003753672

ClinVar Variation:

156107

2907429

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Asn1466Lys	CA170758 NM_014191.4:c.4398C>A CA384908571 NM_014191.4:c.4398C>G