Allele Registry

Canonical Allele Identifier: PA2580124555

Gene: OR2T29 HGNC NCBI

ClinVar RCV:

RCV004138990

ClinVar Variation:

2286946

HGVS (amino-acid)	Matching Registered Transcripts
NP_001004694.2:p.Glu236Ala	CA1505448 NM_001004694.3:c.707A>C