Canonical Allele Identifier: PA2825066370
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 3147928
ClinVar RCV Id: RCV004437761
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp358His
CA9316547
NM_000095.3:c.1072G>C