Canonical Allele Identifier: PA2827761559
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68570

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Ala1772Thr
CA285021
NM_001353949.2:c.5314G>A