Canonical Allele Identifier: PA2828361599
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 640559
ClinVar RCV Id: RCV000793606
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Thr1846Ala
CA384888366
NM_001369788.1:c.5536A>G