Canonical Allele Identifier: PA2499228407
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1055714
ClinVar RCV Id: RCV001364433 RCV003169832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asn132Lys
CA9316731
NM_000095.3:c.396C>G
CA404896763
NM_000095.3:c.396C>A