Canonical Allele Identifier: PA104663
Gene: OCRL HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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