Allele Registry

Canonical Allele Identifier: PA155063

Gene: SCN2A HGNC NCBI

ClinVar RCV:

RCV000118260

RCV000379925

RCV000860054

RCV001640094

RCV002312496

ClinVar Variation:

130224

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035232.1:p.Arg19Lys	CA155062 NM_001040142.2:c.56G>A