Canonical Allele Identifier: PA111577
Gene: OCLN HGNC NCBI

Linked Data

ClinVar Variation Id: 6752
ClinVar RCV Id: RCV000007144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001192183.1:p.Phe219Ser
CA213150
NM_001205254.2:c.656T>C