Canonical Allele Identifier: PA2827291784
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 985603
ClinVar RCV Id: RCV001266596
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Arg1003Cys
CA384892097
NM_001330260.2:c.3007C>T