Canonical Allele Identifier: PA2827363035
Gene: CNTN2 HGNC NCBI
ClinVar RCV:
RCV002216321
ClinVar Variation:
1563151
JSON-LD

Amino-acid Alleles

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