Canonical Allele Identifier: PA2828361669
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1349586
ClinVar RCV Id: RCV002047028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Cys1939Ser
CA384890758
NM_001369788.1:c.5815T>A
CA384890762
NM_001369788.1:c.5816G>C