Canonical Allele Identifier: PA2826130724
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1020583
ClinVar RCV Id: RCV001320182

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Ala1773Gly
CA384886187
NM_001177984.2:c.5318C>G