Canonical Allele Identifier: PA645449574
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 426434
ClinVar RCV Id: RCV000489233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Arg1872Gly
CA384888065
NM_014191.4:c.5614C>G