Canonical Allele Identifier: PA2826130546
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 573377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Met1559Ile
CA384880261
NM_001177984.2:c.4677G>A
CA384880262
NM_001177984.2:c.4677G>C
CA384880263
NM_001177984.2:c.4677G>T