Canonical Allele Identifier: PA645419049
Gene: OCRL HGNC NCBI

Linked Data

ClinVar Variation Id: 384439
ClinVar RCV Id: RCV000434372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000267.2:p.His524Tyr
CA16608732
NM_000276.4:c.1570C>T