Allele Registry

Canonical Allele Identifier: PA2827764838

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000022765

ClinVar Variation:

29884

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340879.1:p.Arg851Gly	CA281752 NM_001353950.2:c.2551C>G