Canonical Allele Identifier: PA213249
Gene: OCLN HGNC NCBI

Linked Data

ClinVar Variation Id: 159460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002529.1:p.Ala151Val
CA213248
NM_002538.4:c.452C>T