Canonical Allele Identifier: PA2826130810
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 546708
ClinVar RCV Id: RCV000658650 RCV001215294
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Arg1850His
CA384888435
NM_001177984.2:c.5549G>A