Canonical Allele Identifier: PA2828361614
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2703903
ClinVar RCV Id: RCV003589774

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Ala1864Thr
CA384888767
NM_001369788.1:c.5590G>A