Allele Registry

Canonical Allele Identifier: PA2826013188

Gene: SCN1A HGNC NCBI

ClinVar Allele:

516552

ClinVar RCV:

RCV000636329

RCV001091664

ClinVar Variation:

530454

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159436.1:p.Leu1323Pro	CA349050683 NM_001165964.3:c.3968T>C