Canonical Allele Identifier: PA2827769068
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1801821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Thr105Asn
CA59804349
NM_001353951.2:c.314C>A