Canonical Allele Identifier: PA2827771031
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 93647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Ala1262Pro
CA221583
NM_001353951.2:c.3784G>C