Allele Registry

Canonical Allele Identifier: PA303547

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000180967

RCV002316981

ClinVar Variation:

190011

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Ala1651Val	CA303545 NM_006920.6:c.4952C>T