Canonical Allele Identifier: PA2827780725
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68649

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Phe1680Ser
CA285207
NM_001353955.2:c.5039T>C