Canonical Allele Identifier: PA658676432
Gene: OSGEP HGNC NCBI

Linked Data

ClinVar Variation Id: 449687
ClinVar RCV Id: RCV000522704 RCV001266639 RCV001335865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060277.1:p.Arg325Trp
CA7081003
NM_017807.4:c.973C>T