Canonical Allele Identifier: PA2826129931
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 2443599

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Met751Thr
CA384879964
NM_001177984.2:c.2252T>C