Allele Registry

Canonical Allele Identifier: PA284894

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059389

ClinVar Variation:

68517

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Asp79His	CA284892 NM_006920.6:c.235G>C