Canonical Allele Identifier: PA2827292617
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 453056
ClinVar RCV Id: RCV000521572
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Asp1724Tyr
CA384884172
NM_001330260.2:c.5170G>T