Allele Registry

Canonical Allele Identifier: PA2826129472

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000189298

RCV001220316

ClinVar Variation:

207140

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171455.1:p.Ala205Glu	CA318317 NM_001177984.2:c.614C>A