Canonical Allele Identifier: PA2826130660
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2170312
ClinVar RCV Id: RCV003080473

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Leu1682Ile
CA384884111
NM_001177984.2:c.5044C>A