Canonical Allele Identifier: PA645418881
Gene: OCRL HGNC NCBI

Linked Data

ClinVar Variation Id: 423653
ClinVar RCV Id: RCV000482529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000267.2:p.Ala9Thr
CA16621196
NM_000276.4:c.25G>A