Allele Registry

Canonical Allele Identifier: PA2828471926

Gene: SCN2A HGNC NCBI

Linked Data

ClinVar RCV:

RCV000189136

RCV000302248

RCV000463410

RCV000655981

RCV000725887

RCV001329197

RCV003224211

RCV003985294

ClinVar Variation:

206987

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358175.1:p.Glu1153Lys	CA317927 NM_001371246.1:c.3457G>A