Canonical Allele Identifier: PA2827771758
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2752271
ClinVar RCV Id: RCV003589992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Ser1679Pro
CA349069400
NM_001353951.2:c.5035T>C