Canonical Allele Identifier: PA2827771021
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68623
ClinVar RCV Id: RCV000059500
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Leu1254Pro
CA285147
NM_001353951.2:c.3761T>C