Allele Registry

Canonical Allele Identifier: PA2827755016

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059537

ClinVar Variation:

68657

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340877.1:p.Tyr1781Cys	CA285228 NM_001353948.2:c.5342A>G