Canonical Allele Identifier: PA2827754644
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 845338
ClinVar RCV Id: RCV001048383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Phe1692Ile
CA349069369
NM_001353948.2:c.5074T>A