Canonical Allele Identifier: PA344891
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 65556
ClinVar RCV Id: RCV002054896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Ser681Cys
CA344890
NM_000095.3:c.2042C>G