Canonical Allele Identifier: PA2827776968
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Arg1233Gln
CA284931
NM_001353954.2:c.3698G>A