Canonical Allele Identifier: PA2827770164
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2801129
ClinVar RCV Id: RCV003753978

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Arg618Ser
CA349067449
NM_001353951.2:c.1852C>A