Allele Registry

Canonical Allele Identifier: PA285080

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059473

RCV000332135

ClinVar Variation:

68596

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Phe90Ser	CA285078 NM_006920.6:c.269T>C