Canonical Allele Identifier: PA2827781590
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2585513
ClinVar RCV Id: RCV003338129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Thr254Ile
CA349073548
NM_001353957.2:c.761C>T