Canonical Allele Identifier: PA916022624
Gene: OCRL HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305713.1:p.His525Gln
CA255585
NM_001318784.2:c.1575C>G
CA414616529
NM_001318784.2:c.1575C>A