Canonical Allele Identifier: PA2827291815
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1039971
ClinVar RCV Id: RCV001343540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Ala1028Gly
CA384892346
NM_001330260.2:c.3083C>G