Canonical Allele Identifier: PA2580107043
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1723871
ClinVar RCV Id: RCV002306432
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp349His
CA404888430
NM_000095.3:c.1045G>C