Canonical Allele Identifier: PA645419056
Gene: OCRL HGNC NCBI

Linked Data

ClinVar Variation Id: 265391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000267.2:p.Pro526Ser
CA10588739
NM_000276.4:c.1576C>T