Allele Registry

Canonical Allele Identifier: PA2829676502

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001195896

RCV001863098

ClinVar Variation:

930321

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Tyr1770His	CA349068092 NM_006920.6:c.5308T>C