Canonical Allele Identifier: PA2828361579
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1679326
ClinVar RCV Id: RCV002226923

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Val1833Leu
CA384888120
NM_001369788.1:c.5497G>C
CA384888123
NM_001369788.1:c.5497G>T