Allele Registry

Canonical Allele Identifier: PA284963

Gene: SCN1A HGNC NCBI

ClinVar Allele:

79436

ClinVar RCV:

RCV000059418

RCV000812820

RCV003224861

ClinVar Variation:

68544

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Pro1440Leu	CA284961 NM_006920.6:c.4319C>T