Canonical Allele Identifier: PA2573162353
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1678031
ClinVar RCV Id: RCV002224622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp494Gly
CA404884101
NM_000095.3:c.1481A>G