Canonical Allele Identifier: PA2827363029
Gene: CNTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1974747
ClinVar RCV Id: RCV002765777
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333012.1:p.Arg72Pro
CA1350953
NM_001346083.2:c.215G>C