Canonical Allele Identifier: PA2826130835
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 1445246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Thr1879Pro
CA384889193
NM_001177984.2:c.5635A>C