Allele Registry

Canonical Allele Identifier: PA2827292140

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000054506

RCV003992171

ClinVar Variation:

60709

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317189.1:p.Leu1331Val	CA144634 NM_001330260.2:c.3991C>G