Canonical Allele Identifier: PA2826130210
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2584848
ClinVar RCV Id: RCV003340748

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Asn1109Lys
CA384893685
NM_001177984.2:c.3327C>A
CA384893686
NM_001177984.2:c.3327C>G