Allele Registry

Canonical Allele Identifier: PA2580124358

Gene: OR13H1 HGNC NCBI

ClinVar RCV:

RCV004171266

ClinVar Variation:

2324673

HGVS (amino-acid)	Matching Registered Transcripts
NP_001004486.1:p.Ile15Ser	CA10518379 NM_001004486.1:c.44T>G