Canonical Allele Identifier: PA2826014025
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2846763
ClinVar RCV Id: RCV003754652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Asp1788Glu
CA349067509
NM_001165964.3:c.5364T>G
CA349067511
NM_001165964.3:c.5364T>A