Canonical Allele Identifier: PA2826130006
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 948943
ClinVar RCV Id: RCV001220301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Leu854Met
CA384886651
NM_001177984.2:c.2560T>A