Allele Registry

Canonical Allele Identifier: PA658659692

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000554528

ClinVar Variation:

461279

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Ser1723Pro	CA349068817 NM_001165963.4:c.5167T>C