Canonical Allele Identifier: PA2827768544
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68573

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Ile1911Thr
CA285030
NM_001353950.2:c.5732T>C