Allele Registry

Canonical Allele Identifier: PA2827765071

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180915

RCV001376917

ClinVar Variation:

189961

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340879.1:p.Arg920Pro	CA303413 NM_001353950.2:c.2759G>C