Canonical Allele Identifier: PA2827292838
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1516533
ClinVar RCV Id: RCV002026670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Leu1890Pro
CA384888421
NM_001330260.2:c.5669T>C