Allele Registry

Canonical Allele Identifier: PA2580126341

Gene: OR9Q2 HGNC NCBI

ClinVar RCV:

RCV004094238

ClinVar Variation:

2233244

HGVS (amino-acid)	Matching Registered Transcripts
NP_001005283.1:p.Val216Ala	CA380722254 NM_001005283.3:c.647T>C