Canonical Allele Identifier: PA645418890
Gene: OCRL HGNC NCBI

Linked Data

ClinVar Variation Id: 436102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000267.2:p.Gly17Ala
CA10511918
NM_000276.4:c.50G>C