Allele Registry

Canonical Allele Identifier: PA2827789734

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV001070909

ClinVar Variation:

863847

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340889.1:p.Pro1719Arg	CA349068404 NM_001353960.2:c.5156C>G