Canonical Allele Identifier: PA916036790
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340890.1:p.Gly619Glu
CA285162
NM_001353961.2:c.1856G>A