Canonical Allele Identifier: PA645471458
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 429931
ClinVar RCV Id: RCV000493700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.His441Arg
CA404885232
NM_000095.3:c.1322A>G