Canonical Allele Identifier: PA2826129557
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 833747

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Gly296Asp
CA385226754
NM_001177984.2:c.887G>A