Canonical Allele Identifier: PA2825066518
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 3147932
ClinVar RCV Id: RCV004437765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Val519Met
CA9316359
NM_000095.3:c.1555G>A