Allele Registry

Canonical Allele Identifier: PA284876

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059380

RCV002345371

RCV002514305

ClinVar Variation:

68508

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Phe403Leu	CA284874 NM_006920.6:c.1207T>C CA349070974 NM_006920.6:c.1209T>G CA349070975 NM_006920.6:c.1209T>A