Canonical Allele Identifier: PA2580106994
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2440511
ClinVar RCV Id: RCV003145856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Cys151Tyr
CA404896433
NM_000095.3:c.452G>A