Allele Registry

Canonical Allele Identifier: PA645449415

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000338932

RCV000636327

RCV001254990

ClinVar Variation:

280470

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Met1481Val	CA10603278 NM_014191.4:c.4441A>G