Canonical Allele Identifier: PA2828360323
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1355892
ClinVar RCV Id: RCV001867154
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Val264Ala
CA385226530
NM_001369788.1:c.791T>C