Canonical Allele Identifier: PA2828361623
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2097452
ClinVar RCV Id: RCV003018820
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Gly1873Asp
CA384889047
NM_001369788.1:c.5618G>A