Allele Registry

Canonical Allele Identifier: PA317579

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000188992

RCV000478480

RCV000806458

ClinVar Variation:

206858

421189

HGVS (amino-acid)	Matching Registered Transcripts
NP_008851.3:p.Phe1696Leu	CA317577 NM_006920.6:c.5088T>A CA16617283 NM_006920.6:c.5088T>G CA349069109 NM_006920.6:c.5086T>C