Canonical Allele Identifier: PA2828361605
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1380899
ClinVar RCV Id: RCV001895105

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Arg1851Leu
CA384888455
NM_001369788.1:c.5552G>T