Allele Registry

Canonical Allele Identifier: PA104663

Gene: OCRL HGNC NCBI

ClinVar RCV:

RCV000059600

ClinVar Variation:

68719

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