Canonical Allele Identifier: PA915987191
Gene: OCRL HGNC NCBI

Linked Data

ClinVar Variation Id: 423653
ClinVar RCV Id: RCV000482529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001578.2:p.Ala9Thr
CA16621196
NM_001587.4:c.25G>A