Allele Registry

Canonical Allele Identifier: PA2827782021

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV002263229

ClinVar Variation:

1694979

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340886.1:p.Tyr545Asp	CA349069088 NM_001353957.2:c.1633T>G