Canonical Allele Identifier: PA2827291829
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1806334
ClinVar RCV Id: RCV002470618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Tyr1038Cys
CA384892499
NM_001330260.2:c.3113A>G