Canonical Allele Identifier: PA2828360919
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1928589
ClinVar RCV Id: RCV002635047
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Arg1026Leu
CA6571542
NM_001369788.1:c.3077G>T