Canonical Allele Identifier: PA916022626
Gene: OCRL HGNC NCBI

Linked Data

ClinVar Variation Id: 265391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305713.1:p.Pro527Ser
CA10588739
NM_001318784.2:c.1579C>T