Canonical Allele Identifier: PA2580322322
Gene: CNTN2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005067.1:p.Arg72Pro
CA1350953
NM_005076.5:c.215G>C