Canonical Allele Identifier: PA2826130208
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 833718
ClinVar RCV Id: RCV001034202

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Asn1107His
CA384893632
NM_001177984.2:c.3319A>C