Canonical Allele Identifier: PA2826130804
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 588808
ClinVar RCV Id: RCV002315304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Ile1845Val
CA384888351
NM_001177984.2:c.5533A>G