Canonical Allele Identifier: PA2827363035
Gene: CNTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1563151
ClinVar RCV Id: RCV002216321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333012.1:p.Met80Val
CA1350983
NM_001346083.2:c.238A>G