Canonical Allele Identifier: PA2826013038
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206808
ClinVar RCV Id: RCV000188928

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Val1230Ile
CA317395
NM_001165964.3:c.3688G>A