Canonical Allele Identifier: PA658654568
Gene: OSGEP HGNC NCBI

Linked Data

ClinVar Variation Id: 444886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060277.1:p.Arg325Gln
CA7081001
NM_017807.4:c.974G>A