Canonical Allele Identifier: PA2826012623
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68524

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Gly922Glu
CA284913
NM_001165964.3:c.2765G>A