Canonical Allele Identifier: PA2826130151
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1003965
ClinVar RCV Id: RCV001300588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Asn1047Ser
CA6571551
NM_001177984.2:c.3140A>G