Canonical Allele Identifier: PA2826130142
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2845017
ClinVar RCV Id: RCV003754622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Ala1042Thr
CA384892566
NM_001177984.2:c.3124G>A