Allele Registry

Canonical Allele Identifier: PA2827292668

Gene: SCN8A HGNC NCBI

ClinVar RCV:

RCV000023031

RCV001230237

RCV003992161

ClinVar Variation:

30123

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317189.1:p.Asn1768Asp	CA128948 NM_001330260.2:c.5302A>G