Canonical Allele Identifier: PA2573241687
Gene: CNTN2 HGNC NCBI
ClinVar RCV:
RCV001969516
ClinVar Variation:
1473378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005067.1:p.Leu11Val
CA344402490
NM_005076.5:c.31C>G