Canonical Allele Identifier: PA2827363055
Gene: CNTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 474483
ClinVar RCV Id: RCV000552208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333012.1:p.Val120Ile
CA344405319
NM_001346083.2:c.358G>A