Canonical Allele Identifier: PA2827762154
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 206884

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Ile1950Thr
CA317678
NM_001353949.2:c.5849T>C