Canonical Allele Identifier: PA104482
Gene: OCRL HGNC NCBI

Linked Data

ClinVar Variation Id: 68708
ClinVar RCV Id: RCV000059589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000267.2:p.Arg457Gly
CA266151
NM_000276.4:c.1369C>G