Allele Registry

Canonical Allele Identifier: PA2826129984

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000232244

ClinVar Variation:

240885

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171455.1:p.Leu840Arg	CA10583048 NM_001177984.2:c.2519T>G