Canonical Allele Identifier: PA2826130827
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2957635
ClinVar RCV Id: RCV003811298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Arg1872Gln
CA384889029
NM_001177984.2:c.5615G>A