Canonical Allele Identifier: PA2827363024
Gene: CNTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1994929
ClinVar RCV Id: RCV002791498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333012.1:p.Arg64Trp
CA36428387
NM_001346083.2:c.190C>T