Canonical Allele Identifier: PA2826129474
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 207145

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171455.1:p.Ile207Val
CA318327
NM_001177984.2:c.619A>G