Canonical Allele Identifier: PA2827292834
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 588808
ClinVar RCV Id: RCV002315304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Ile1886Val
CA384888351
NM_001330260.2:c.5656A>G