Canonical Allele Identifier: PA916012251
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 656459
ClinVar RCV Id: RCV000812885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ser1882Tyr
CA384888287
NM_014191.4:c.5645C>A