Canonical Allele Identifier: PA2827750008
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Thr297Ile
CA285264
NM_001353948.2:c.890C>T