Canonical Allele Identifier: PA2826370654
Gene: CNTN1 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242992.1:p.Ala427Gly
CA6516829
NM_001256063.2:c.1280C>G