Canonical Allele Identifier: PA2826279398
Gene: OCLN HGNC NCBI

Linked Data

ClinVar Variation Id: 211776

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001192183.1:p.Arg66Leu
CA208038
NM_001205254.2:c.197G>T