Canonical Allele Identifier: PA645471466
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 420111
ClinVar RCV Id: RCV000483120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp511Glu
CA16620813
NM_000095.3:c.1533C>G
CA404883483
NM_000095.3:c.1533C>A