Canonical Allele Identifier: PA2826129912
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 945997
ClinVar RCV Id: RCV001216764
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Cys722Trp
CA384879757
NM_001177984.2:c.2166C>G