Canonical Allele Identifier: PA2827771065
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2104158
ClinVar RCV Id: RCV003031242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Ser1284Pro
CA349053536
NM_001353951.2:c.3850T>C