Canonical Allele Identifier: PA2826130805
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_001171455.1:p.Thr1846Ala
CA384888366
NM_001177984.2:c.5536A>G