Canonical Allele Identifier: PA2827771869
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 863847
ClinVar RCV Id: RCV001070909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Pro1737Arg
CA349068404
NM_001353951.2:c.5210C>G