Allele Registry

Canonical Allele Identifier: PA2827749639

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000498818

RCV001857000

ClinVar Variation:

431844

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340877.1:p.Asn211Ser	CA349074293 NM_001353948.2:c.632A>G