Canonical Allele Identifier: PA343854
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 40988
ClinVar RCV Id: RCV000033880 RCV000486037 RCV001332185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp473del