Canonical Allele Identifier: PA2828360345
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1675496
ClinVar RCV Id: RCV002211225

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Asn287His
CA385226680
NM_001369788.1:c.859A>C