Canonical Allele Identifier: PA2827363024
Gene: CNTN2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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