Canonical Allele Identifier: PA2580106992
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2007121
ClinVar RCV Id: RCV002842083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Pro147Leu
CA306258911
NM_000095.3:c.440C>T