Allele Registry

Canonical Allele Identifier: PA303199

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180835

ClinVar Variation:

189882

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Arg935Pro	CA303197 NM_006920.6:c.2804G>C