Canonical Allele Identifier: PA113059
Gene: OSMR HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003990.1:p.Gly618Ala
CA119094
NM_003999.3:c.1853G>C