Canonical Allele Identifier: PA2827292936
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2183629
ClinVar RCV Id: RCV002627806
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Arg1968Thr
CA384890437
NM_001330260.2:c.5903G>C