Canonical Allele Identifier: PA2573241710
Gene: CNTN2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005067.1:p.Met80Val
CA1350983
NM_005076.5:c.238A>G