Canonical Allele Identifier: PA2827786891
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 859283
ClinVar RCV Id: RCV001065356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Phe1787Ser
CA349067529
NM_001353958.2:c.5360T>C