Canonical Allele Identifier: PA2827290931
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1044885
ClinVar RCV Id: RCV001349205

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Val283Met
CA385226653
NM_001330260.2:c.847G>A