Canonical Allele Identifier: PA2828361598
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 588808
ClinVar RCV Id: RCV002315304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Ile1845Val
CA384888351
NM_001369788.1:c.5533A>G