Allele Registry

Canonical Allele Identifier: PA2828470605

Gene: SCN2A HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000022769

RCV000118251

RCV000189193

RCV000416960

RCV001035869

RCV001200935

RCV001265272

RCV003155911

RCV003985263

ClinVar Variation:

29888

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358175.1:p.Ala263Val	CA128711 NM_001371246.1:c.788C>T