Canonical Allele Identifier: PA2827362995
Gene: CNTN2 HGNC NCBI
ClinVar RCV:
RCV001969516
ClinVar Variation:
1473378
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333012.1:p.Leu11Val
CA344402490
NM_001346083.2:c.31C>G