Canonical Allele Identifier: PA2580102146
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2098882
ClinVar RCV Id: RCV003019332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Pro633Leu
CA306253509
NM_000095.3:c.1898C>T