Allele Registry

Canonical Allele Identifier: PA2827790149

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000539521

ClinVar Variation:

461252

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Thr27Arg	CA349062549 NM_001353961.2:c.80C>G