Allele Registry

Canonical Allele Identifier: PA2826259645

Gene: SCN1A HGNC NCBI

ClinVar Allele:

99549

ClinVar RCV:

RCV000079577

RCV000701047

RCV002345392

RCV003155068

ClinVar Variation:

93645

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Phe1259Ser	CA285448 NM_001202435.3:c.3776T>C