Allele Registry

Canonical Allele Identifier: PA2829676556

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001045336

ClinVar Variation:

842847

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Phe1804Leu	CA349067524 NM_006920.6:c.5412T>G CA349067526 NM_006920.6:c.5412T>A CA349067536 NM_006920.6:c.5410T>C