Canonical Allele Identifier: PA2828360890
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 976416
ClinVar RCV Id: RCV001253721
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Asp989Tyr
CA384891939
NM_001369788.1:c.2965G>T