Canonical Allele Identifier: PA2826130163
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 436670
ClinVar RCV Id: RCV000503487 RCV000763860 RCV001305760 RCV001584221
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Arg1055Gln
CA6571555
NM_001177984.2:c.3164G>A