Canonical Allele Identifier: PA2827290925
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2894009
ClinVar RCV Id: RCV003753026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Arg278Gln
CA385226620
NM_001330260.2:c.833G>A