Canonical Allele Identifier: PA1139740458
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 859283
ClinVar RCV Id: RCV001065356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Phe1815Ser
CA349067529
NM_001353948.2:c.5444T>C