Allele Registry

Canonical Allele Identifier: PA317782

Gene: SCN1A HGNC NCBI

ClinVar Variation Id: 206935

ClinVar RCV Id: RCV000189079

ClinVar Variation Id: 2846673

ClinVar RCV Id: RCV003754649

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Phe402Leu	CA317779 NM_006920.6:c.1204T>C CA349070981 NM_006920.6:c.1206T>G CA349070982 NM_006920.6:c.1206T>A