Canonical Allele Identifier: PA113077
Gene: OSMR HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003990.1:p.Lys697Thr
CA129037
NM_003999.3:c.2090A>C