Allele Registry

Canonical Allele Identifier: PA2829675252

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000413718

ClinVar Variation:

372972

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Leu858Ser	CA16042442 NM_006920.6:c.2573T>C