Canonical Allele Identifier: PA2741808975
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2530623
ClinVar RCV Id: RCV003290959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Phe531Leu
CA404882987
NM_000095.3:c.1593C>G
CA404882991
NM_000095.3:c.1593C>A
CA404883006
NM_000095.3:c.1591T>C