Allele Registry

Canonical Allele Identifier: PA2827772577

Gene: SCN1A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

79470

ClinVar RCV:

RCV000059454

RCV000188843

RCV000558296

RCV000763460

RCV001003956

RCV001420531

RCV002470755

RCV003764743

ClinVar Variation:

68578

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340881.1:p.Thr226Met	CA285042 NM_001353952.2:c.677C>T