Canonical Allele Identifier: PA2828361513
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 207129
ClinVar RCV Id: RCV000189287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Cys1765Tyr
CA318296
NM_001369788.1:c.5294G>A