Canonical Allele Identifier: PA2826129552
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1675496
ClinVar RCV Id: RCV002211225

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Asn287His
CA385226680
NM_001177984.2:c.859A>C