Canonical Allele Identifier: PA104663
Gene: OCRL HGNC NCBI

Linked Data

ClinVar Variation Id: 68719
ClinVar RCV Id: RCV000059600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000267.2:p.His524Arg
CA266161
NM_000276.4:c.1571A>G