Canonical Allele Identifier: PA2827291862
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 130245

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Ile1053Ser
CA231493
NM_001330260.2:c.3158T>G