Canonical Allele Identifier: PA2825272197
Gene: OR10G2 HGNC NCBI
ClinVar RCV:
RCV004499388
ClinVar Variation:
3204501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005466.2:p.Arg170Cys
CA7094437
NM_001005466.2:c.508C>T