Canonical Allele Identifier: PA2826130121
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1339139

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Gln1020His
CA10641732
NM_001177984.2:c.3060G>C
CA384892233
NM_001177984.2:c.3060G>T