Canonical Allele Identifier: PA2826130134
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 391947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Val1031Ala
CA16606571
NM_001177984.2:c.3092T>C