Allele Registry

Canonical Allele Identifier: PA2827770873

Gene: SCN1A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

79508

ClinVar RCV:

RCV000059493

RCV000188915

RCV000296106

RCV000415355

RCV000655982

RCV000723551

RCV000986890

RCV001082811

RCV001129578

RCV002313744

RCV004537267

ClinVar Variation:

68616

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340880.1:p.Thr1163Ser	CA221580 NM_001353951.2:c.3488C>G CA349056646 NM_001353951.2:c.3487A>T