Canonical Allele Identifier: PA2826129611
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1686170
ClinVar RCV Id: RCV002250337

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Gly384Arg
CA385227533
NM_001177984.2:c.1150G>A
CA385227535
NM_001177984.2:c.1150G>C