Canonical Allele Identifier: PA2580102139
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2338079
ClinVar RCV Id: RCV002950261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Val580Leu
CA404879202
NM_000095.3:c.1738G>C
CA404879204
NM_000095.3:c.1738G>T