Canonical Allele Identifier: PA2499278045
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1020583
ClinVar RCV Id: RCV001320182

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ala1814Gly
CA384886187
NM_014191.4:c.5441C>G