Canonical Allele Identifier: PA916026851
Gene: OSMR HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310435.1:p.Ile692Thr
CA119093
NM_001323506.2:c.2075T>C