Canonical Allele Identifier: PA2827790831
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1715838
ClinVar RCV Id: RCV002304639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Phe1126Tyr
CA349063678
NM_001353961.2:c.3377T>A