Allele Registry

Canonical Allele Identifier: PA2827772363

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059473

RCV000332135

ClinVar Variation:

68596

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340881.1:p.Phe90Ser	CA285078 NM_001353952.2:c.269T>C