Allele Registry

Canonical Allele Identifier: PA645449401

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000480970

RCV000988848

RCV001856819

ClinVar Variation:

418482

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Gly1476Ser	CA16619563 NM_014191.4:c.4426G>A