Allele Registry

Canonical Allele Identifier: PA2580126988

Gene: OR6C68 HGNC NCBI

ClinVar RCV:

RCV004224795

ClinVar Variation:

2387936

HGVS (amino-acid)	Matching Registered Transcripts
NP_001005519.2:p.Met116Val	CA6614234 NM_001005519.2:c.346A>G