Allele Registry

Canonical Allele Identifier: PA2827772392

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180910

ClinVar Variation:

189956

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340881.1:p.Leu108Pro	CA303399 NM_001353952.2:c.323T>C