Canonical Allele Identifier: PA100251
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 9189
ClinVar RCV Id: RCV000009767 RCV001851774 RCV002054430
ClinVar Variation Id: 432270
ClinVar RCV Id: RCV000498353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asn523Lys
CA120167
NM_000095.3:c.1569C>G
CA404883154
NM_000095.3:c.1569C>A