Canonical Allele Identifier: PA2827762098
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1715838
ClinVar RCV Id: RCV002304639
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Phe1929Tyr
CA349063678
NM_001353949.2:c.5786T>A