Canonical Allele Identifier: PA916022608
Gene: OCRL HGNC NCBI

Linked Data

ClinVar Variation Id: 68710
ClinVar RCV Id: RCV000059591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305713.1:p.Glu469Lys
CA266153
NM_001318784.2:c.1405G>A