Canonical Allele Identifier: PA2827767996
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2571621
ClinVar RCV Id: RCV003313331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Ser1749Tyr
CA349068298
NM_001353950.2:c.5246C>A