Canonical Allele Identifier: PA100641
Gene: COMP HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Gly299Arg
CA404891554
NM_000095.3:c.895G>C
CA404891559
NM_000095.3:c.895G>A