Canonical Allele Identifier: PA340881
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 9193
ClinVar RCV Id: RCV000009771 RCV000033881 RCV001090556 RCV002054431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp473dup