Allele Registry

Canonical Allele Identifier: PA318289

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV003588503

ClinVar Variation:

2735862

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Leu1630Pro	CA318288 NM_014191.4:c.4889T>C