Canonical Allele Identifier: PA658817177
Gene: OSGEP HGNC NCBI

Linked Data

ClinVar Variation Id: 521157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060277.1:p.Val107Met
CA7081272
NM_017807.4:c.319G>A