Allele Registry

Canonical Allele Identifier: PA2829675666

Gene: SCN1A HGNC NCBI

ClinVar Variation Id: 1064343

ClinVar RCV Id: RCV001374298

ClinVar Variation Id: 2498837

ClinVar RCV Id: RCV003223046

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Phe1209Leu	CA349055932 NM_006920.6:c.3627T>G CA349055935 NM_006920.6:c.3627T>A CA349055945 NM_006920.6:c.3625T>C