Canonical Allele Identifier: PA2827785864
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2581808

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Gly1205Ser
CA349055647
NM_001353958.2:c.3613G>A