Canonical Allele Identifier: PA2827780559
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68554

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Asp1596Tyr
CA284982
NM_001353955.2:c.4786G>T