Canonical Allele Identifier: PA916022567
Gene: OCRL HGNC NCBI

Linked Data

ClinVar Variation Id: 436102
ClinVar RCV Id: RCV000502299 RCV002056860 RCV003992307 RCV004023389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305713.1:p.Gly18Ala
CA10511918
NM_001318784.2:c.53G>C