Allele Registry

Canonical Allele Identifier: PA2826260559

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059537

ClinVar Variation:

68657

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189364.1:p.Tyr1781Cys	CA285228 NM_001202435.3:c.5342A>G