Allele Registry

Canonical Allele Identifier: PA2826012115

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV002263229

ClinVar Variation:

1694979

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Tyr545Asp	CA349069088 NM_001165964.3:c.1633T>G