Canonical Allele Identifier: PA2827769654
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 846430
ClinVar RCV Id: RCV001049730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Leu263Pro
CA349073370
NM_001353951.2:c.788T>C