Canonical Allele Identifier: PA2826130809
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2975016
ClinVar RCV Id: RCV003838638
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Arg1850Cys
CA6571939
NM_001177984.2:c.5548C>T