Canonical Allele Identifier: PA2826013791
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 845338
ClinVar RCV Id: RCV001048383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Phe1664Ile
CA349069369
NM_001165964.3:c.4990T>A