Allele Registry

Canonical Allele Identifier: PA2826012553

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000487225

RCV000636316

ClinVar Variation:

422367

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Gln882Arg	CA16617303 NM_001165964.3:c.2645A>G