Canonical Allele Identifier: PA2827292596
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1183709
ClinVar RCV Id: RCV001541613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317189.1:p.Ser1704Thr
CA384883405
NM_001330260.2:c.5110T>A