Allele Registry

Canonical Allele Identifier: PA2580336408

Gene: OMP HGNC NCBI

ClinVar RCV:

RCV004122681

ClinVar Variation:

2265753

HGVS (amino-acid)	Matching Registered Transcripts
NP_006180.1:p.Leu163Pro	CA6196383 NM_006189.1:c.488T>C