Canonical Allele Identifier: PA2828361571
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 420831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Met1828Thr
CA16619566
NM_001369788.1:c.5483T>C