Allele Registry

Canonical Allele Identifier: PA2827786965

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000636288

ClinVar Variation:

530427

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340887.1:p.Asp1838Gly	CA16602232 NM_001353958.2:c.5513A>G