Canonical Allele Identifier: PA2827292850
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2703903
ClinVar RCV Id: RCV003589774

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Ala1905Thr
CA384888767
NM_001330260.2:c.5713G>A