Allele Registry

Canonical Allele Identifier: PA891849224

Gene: CNTN2 HGNC NCBI

ClinVar RCV:

RCV000693800

RCV004025168

ClinVar Variation:

572426

HGVS (amino-acid)	Matching Registered Transcripts
NP_005067.1:p.Arg914Gln	CA1351792 NM_005076.5:c.2741G>A