Canonical Allele Identifier: PA916026850
Gene: OSMR HGNC NCBI
ClinVar Allele:
39176
ClinVar RCV:
RCV000023143
ClinVar Variation:
30220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310435.1:p.Asp648Val
CA129035
NM_001323506.2:c.1943A>T