Canonical Allele Identifier: PA2826130096
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 932333
ClinVar RCV Id: RCV001200086
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Asp989Val
CA384891942
NM_001177984.2:c.2966A>T