Canonical Allele Identifier: PA2827363003
Gene: CNTN2 HGNC NCBI
ClinVar RCV:
RCV002570901
ClinVar Variation:
1899799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333012.1:p.Leu29Val
CA1350926
NM_001346083.2:c.85C>G