Canonical Allele Identifier: PA916022614
Gene: OCRL HGNC NCBI

Linked Data

ClinVar Variation Id: 10858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305713.1:p.Arg501Gln
CA255583
NM_001318784.2:c.1502G>A