Canonical Allele Identifier: PA104502
Gene: OCRL HGNC NCBI

Linked Data

ClinVar Variation Id: 10858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000267.2:p.Arg500Gln
CA255583
NM_000276.4:c.1499G>A