Canonical Allele Identifier: PA2828360915
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1339139

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Gln1020His
CA10641732
NM_001369788.1:c.3060G>C
CA384892233
NM_001369788.1:c.3060G>T