Canonical Allele Identifier: PA2573162362
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1476680
ClinVar RCV Id: RCV001998184
ClinVar Variation Id: 2992629
ClinVar RCV Id: RCV003857740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp544Glu
CA9316343
NM_000095.3:c.1632C>G
CA9316344
NM_000095.3:c.1632C>A