Canonical Allele Identifier: PA658654562
Gene: OSGEP HGNC NCBI

Linked Data

ClinVar Variation Id: 444888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060277.1:p.Gly177Ala
CA7081183
NM_017807.4:c.530G>C