Canonical Allele Identifier: PA2827771836
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 834858
ClinVar RCV Id: RCV001035628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Asp1716Tyr
CA349068756
NM_001353951.2:c.5146G>T