Canonical Allele Identifier: PA113049
Gene: OSMR HGNC NCBI

Linked Data

ClinVar Variation Id: 30220
ClinVar RCV Id: RCV000023143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003990.1:p.Asp647Val
CA129035
NM_003999.3:c.1940A>T