Canonical Allele Identifier: PA2826130720
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 207129
ClinVar RCV Id: RCV000189287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Cys1765Tyr
CA318296
NM_001177984.2:c.5294G>A