Allele Registry

Canonical Allele Identifier: PA2826258000

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059473

RCV000332135

ClinVar Variation:

68596

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Phe90Ser	CA285078 NM_001202435.3:c.269T>C