Canonical Allele Identifier: PA2826130113
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2507235
ClinVar RCV Id: RCV003239126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Lys1012Thr
CA384892157
NM_001177984.2:c.3035A>C