Canonical Allele Identifier: PA2827292763
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1315611
ClinVar RCV Id: RCV001755273

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Val1855Asp
CA384887577
NM_001330260.2:c.5564T>A