Canonical Allele Identifier: PA232168
Gene: OR9I1 HGNC NCBI

Linked Data

ClinVar Variation Id: 91923
ClinVar RCV Id: RCV000122480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005211.1:p.Tyr73Cys
CA232167
NM_001005211.2:c.218A>G