Canonical Allele Identifier: PA2826279426
Gene: OCLN HGNC NCBI

Linked Data

ClinVar Variation Id: 159460
ClinVar RCV Id: RCV000146971 RCV000425727 RCV002055909 RCV003905271
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001192183.1:p.Ala151Val
CA213248
NM_001205254.2:c.452C>T