Allele Registry

Canonical Allele Identifier: PA2827291589

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000232244

ClinVar Variation:

240885

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317189.1:p.Leu840Arg	CA10583048 NM_001330260.2:c.2519T>G