Canonical Allele Identifier: PA645471415
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 328623
ClinVar RCV Id: RCV000275499 RCV000330560 RCV001435909 RCV002278507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Phe137Ser
CA9316729
NM_000095.3:c.410T>C