Canonical Allele Identifier: PA2827292937
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2444693
ClinVar RCV Id: RCV003154141
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Arg1971Gly
CA384890509
NM_001330260.2:c.5911A>G