Canonical Allele Identifier: PA2829379530
Gene: OCLN HGNC NCBI

Linked Data

ClinVar Variation Id: 1283292
ClinVar RCV Id: RCV001696436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002529.1:p.Val308Leu
CA3294546
NM_002538.4:c.922G>C
CA360066486
NM_002538.4:c.922G>T