Canonical Allele Identifier: PA344887
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 65554
ClinVar RCV Id: RCV002054894
ClinVar Variation Id: 1709017
ClinVar RCV Id: RCV002288301 RCV003097765
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asn555Lys
CA344886
NM_000095.3:c.1665C>A
CA404882077
NM_000095.3:c.1665C>G