Canonical Allele Identifier: PA2826130103
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 576451
ClinVar RCV Id: RCV001542340 RCV000698952
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Asn995Asp
CA384892040
NM_001177984.2:c.2983A>G