Canonical Allele Identifier: PA2829332019
Gene: OCRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1407400
ClinVar RCV Id: RCV001918423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001578.2:p.Ala529Thr
CA414616555
NM_001587.4:c.1585G>A