Canonical Allele Identifier: PA2827771492
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1382067
ClinVar RCV Id: RCV001922132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Gly1521Arg
CA349072354
NM_001353951.2:c.4561G>A
CA349072356
NM_001353951.2:c.4561G>C