Allele Registry

Canonical Allele Identifier: PA2827763062

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000636289

ClinVar Variation:

530428

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340879.1:p.Met251Arg	CA349073597 NM_001353950.2:c.752T>G