Allele Registry

Canonical Allele Identifier: PA916037006

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059537

ClinVar Variation:

68657

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340890.1:p.Tyr967Cys	CA285228 NM_001353961.2:c.2900A>G