Canonical Allele Identifier: PA2827292871
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1316357
ClinVar RCV Id: RCV001766263

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Phe1915Ser
CA384889072
NM_001330260.2:c.5744T>C