Allele Registry

Canonical Allele Identifier: PA303402

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180910

ClinVar Variation:

189956

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Leu108Pro	CA303399 NM_006920.6:c.323T>C