Canonical Allele Identifier: PA2827785487
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Arg918His
CA284910
NM_001353958.2:c.2753G>A