Canonical Allele Identifier: PA915954025
Gene: OR13C5 HGNC NCBI

Linked Data

ClinVar Variation Id: 768317
ClinVar RCV Id: RCV000947195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001004482.1:p.Pro79Ser
CA5166154
NM_001004482.1:c.235C>T