Canonical Allele Identifier: PA2827786657
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 845338
ClinVar RCV Id: RCV001048383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Phe1664Ile
CA349069369
NM_001353958.2:c.4990T>A