Canonical Allele Identifier: PA2826011111
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 859283
ClinVar RCV Id: RCV001065356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Phe1815Ser
CA349067529
NM_001165963.4:c.5444T>C