Canonical Allele Identifier: PA100229
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 9198
ClinVar RCV Id: RCV000009776 RCV001268837 RCV001289465 RCV002054432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Arg718Trp
CA340882
NM_000095.3:c.2152C>T