Canonical Allele Identifier: PA100438
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 9183
ClinVar RCV Id: RCV000009761
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp472Tyr
CA254700
NM_000095.3:c.1414G>T