Canonical Allele Identifier: PA2580126613
Gene: OR10G2 HGNC NCBI
ClinVar RCV:
RCV004161515
ClinVar Variation:
2316582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005466.2:p.Thr14Arg
CA257573451
NM_001005466.2:c.41C>G