Allele Registry

Canonical Allele Identifier: PA2827363067

Gene: CNTN2 HGNC NCBI

ClinVar RCV:

RCV001522165

ClinVar Variation:

1170111

HGVS (amino-acid)	Matching Registered Transcripts
NP_001333012.1:p.Ala145Thr	CA1351047 NM_001346083.2:c.433G>A