Canonical Allele Identifier: PA1139698575
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 890743
ClinVar RCV Id: RCV001125544 RCV001125543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Pro541Ala
CA404882579
NM_000095.3:c.1621C>G