Canonical Allele Identifier: PA658681983
Gene: CNTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 474483
ClinVar RCV Id: RCV000552208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005067.1:p.Val120Ile
CA344405319
NM_005076.5:c.358G>A