Canonical Allele Identifier: PA891855371
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 582453
ClinVar RCV Id: RCV000706526
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055006.1:p.Ala1831Thr
CA6571925
NM_014191.4:c.5491G>A