Canonical Allele Identifier: PA2499228432
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1058021
ClinVar RCV Id: RCV001367108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp479His
CA404884385
NM_000095.3:c.1435G>C