Canonical Allele Identifier: PA2741808971
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2544747
ClinVar RCV Id: RCV003292252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp506Glu
CA9316368
NM_000095.3:c.1518C>G
CA404883645
NM_000095.3:c.1518C>A