Canonical Allele Identifier: PA2827292702
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1411616
ClinVar RCV Id: RCV001920737
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Asp1798Asn
CA384885823
NM_001330260.2:c.5392G>A