Canonical Allele Identifier: PA658654558
Gene: OSGEP HGNC NCBI

Linked Data

ClinVar Variation Id: 444889
ClinVar RCV Id: RCV000513299 RCV001268300 RCV001849392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060277.1:p.Ile14Phe
CA389127659
NM_017807.4:c.40A>T