Canonical Allele Identifier: PA284900
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68519
ClinVar RCV Id: RCV000059391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Glu835Lys
CA284898
NM_006920.6:c.2503G>A