Canonical Allele Identifier: PA100531
Gene: COMP HGNC NCBI
ClinVar RCV:
RCV000009766
ClinVar Variation:
9188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Cys328Arg
CA254702
NM_000095.3:c.982T>C