Allele Registry

Canonical Allele Identifier: PA2580336404

Gene: OMP HGNC NCBI

ClinVar RCV:

RCV004236815

ClinVar Variation:

2402872

HGVS (amino-acid)	Matching Registered Transcripts
NP_006180.1:p.Leu91Phe	CA6196333 NM_006189.1:c.271C>T