Canonical Allele Identifier: PA2826130159
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 975895
ClinVar RCV Id: RCV001253024
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Asp1052Asn
CA384892725
NM_001177984.2:c.3154G>A