Allele Registry

Canonical Allele Identifier: PA2827789685

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059441

ClinVar Variation:

68566

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340889.1:p.Thr1692Arg	CA285009 NM_001353960.2:c.5075C>G