Allele Registry

Canonical Allele Identifier: PA2827780122

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000636329

RCV001091664

ClinVar Variation:

530454

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340884.1:p.Leu1339Pro	CA349050683 NM_001353955.2:c.4016T>C