Canonical Allele Identifier: PA645449392
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 374375
ClinVar RCV Id: RCV000415327

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Asn1468Ser
CA16043682
NM_014191.4:c.4403A>G