Canonical Allele Identifier: PA2826129969
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1325768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Gly822Arg
CA384884105
NM_001177984.2:c.2464G>A
CA384884108
NM_001177984.2:c.2464G>C