Canonical Allele Identifier: PA915956762
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 808505
ClinVar RCV Id: RCV000996825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Cys328Trp
CA404890417
NM_000095.3:c.984C>G