Canonical Allele Identifier: PA208039
Gene: OCLN HGNC NCBI

Linked Data

ClinVar Variation Id: 211776

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002529.1:p.Arg66Leu
CA208038
NM_002538.4:c.197G>T