Allele Registry

Canonical Allele Identifier: PA2826260377

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000441570

RCV002522649

ClinVar Variation:

391762

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Ala1685Ser	CA1942700 NM_001202435.3:c.5053G>T