Allele Registry

Canonical Allele Identifier: PA2827780891

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059537

ClinVar Variation:

68657

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340884.1:p.Tyr1769Cys	CA285228 NM_001353955.2:c.5306A>G