Canonical Allele Identifier: PA2827292614
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2162336
ClinVar RCV Id: RCV003091228

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Leu1723Val
CA384884126
NM_001330260.2:c.5167C>G