Allele Registry

Canonical Allele Identifier: PA2828361241

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000338932

RCV000636327

RCV001254990

ClinVar Variation:

280470

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356717.1:p.Met1440Val	CA10603278 NM_001369788.1:c.4318A>G