Canonical Allele Identifier: PA915940954
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 807399
ClinVar RCV Id: RCV000995525 RCV001597240
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Glu457del
CA915952950
NM_000095.3:c.1371_1373del