Canonical Allele Identifier: PA2826130792
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2575995
ClinVar RCV Id: RCV003322056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Ser1838Tyr
CA384888251
NM_001177984.2:c.5513C>A