Canonical Allele Identifier: PA2826279480
Gene: OCLN HGNC NCBI

Linked Data

ClinVar Variation Id: 2434486
ClinVar RCV Id: RCV003133101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001192183.1:p.Tyr315Phe
CA360066567
NM_001205254.2:c.944A>T