Allele Registry

Canonical Allele Identifier: PA317887

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000189120

RCV000640628

RCV001847838

ClinVar Variation:

206972

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035232.1:p.Leu886Ser	CA317886 NM_001040142.2:c.2657T>C