Allele Registry

Canonical Allele Identifier: PA108011

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059439

ClinVar Variation:

68564

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159435.1:p.Met1714Arg	CA285003 NM_001165963.4:c.5141T>G