Canonical Allele Identifier: PA2827770427
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68519
ClinVar RCV Id: RCV000059391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Glu835Lys
CA284898
NM_001353951.2:c.2503G>A