Canonical Allele Identifier: PA2828361568
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2123352
ClinVar RCV Id: RCV003035370
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Gln1827Pro
CA384887941
NM_001369788.1:c.5480A>C