Allele Registry

Canonical Allele Identifier: PA658807898

Gene: SCN8A HGNC NCBI

ClinVar Allele:

514022

ClinVar RCV:

RCV000626917

RCV000701379

RCV001330491

ClinVar Variation:

523505

HGVS (amino-acid)	Matching Registered Transcripts
NP_055006.1:p.Phe1412Ser	CA384907172 NM_014191.4:c.4235T>C